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nsv4377863

  • Variant Calls:57
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:25,603

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 541 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):51,628,547-51,654,149Question Mark
Overlapping variant regions from other studies: 541 SVs from 77 studies. See in: genome view    
Submitted genomic52,131,800-52,157,402Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4377863RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1951,628,54751,654,149
nsv4377863Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000019.9Chr1952,131,80052,157,402

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15611681copy number loss1-0653-002SNP arrayGenotyping28
nssv15612794copy number loss1-0653-004SNP arrayGenotyping27
nssv15613062copy number loss1-0662-004SNP arrayGenotyping21
nssv15613495copy number loss1-0685-003SNP arrayGenotyping20
nssv15614286copy number loss1-0718-003SNP arrayGenotyping35
nssv15615025copy number loss1-0737-003SNP arrayGenotyping16
nssv15615405copy number loss1-0771-003SNP arrayGenotyping20
nssv15615648copy number loss1-0760-003SNP arrayGenotyping22
nssv15616929copy number loss1-0826-003SNP arrayGenotyping27
nssv15617286copy number loss1-0832-003SNP arrayGenotyping21
nssv15617463copy number loss1-0845-003SNP arrayGenotyping36
nssv15618110copy number loss1-0884-003SNP arrayGenotyping33
nssv15620810copy number loss1-0958-003SNP arrayGenotyping22
nssv15623661copy number loss1-0271-002SNP arrayGenotyping37
nssv15624100copy number loss1-0291-002SNP arrayGenotyping30
nssv15625935copy number loss1-0432-005SNP arrayGenotyping21
nssv15626019copy number loss1-0405-003SNP arrayGenotyping16
nssv15626277copy number loss1-0442-001SNP arrayGenotyping18
nssv15626899copy number loss1-0456-004SNP arrayGenotyping23
nssv15628282copy number loss1-0509-003SNP arrayGenotyping16
nssv15628855copy number loss1-0559-002SNP arrayGenotyping20
nssv15629270copy number loss1-0576-001SNP arrayGenotyping19
nssv15629478copy number loss1-0560-003SNP arrayGenotyping21
nssv15629787copy number loss1-0578-003SNP arrayGenotyping24
nssv15630204copy number loss1-0555-002SNP arrayGenotyping27
nssv15630650copy number loss1-0600-003SNP arrayGenotyping25
nssv15630732copy number loss1-0619-003SNP arrayGenotyping25
nssv15631550copy number loss1-0638-001SNP arrayGenotyping12
nssv15632767copy number loss10-0008-001SNP arrayGenotyping27
nssv15633251copy number loss11-0016-003SNP arrayGenotyping23
nssv15635255copy number loss12-4139-003SNP arrayGenotyping27
nssv15640919copy number loss14-0318-003SNP arrayGenotyping19
nssv15642184copy number loss16-1002-001SNP arrayGenotyping20
nssv15645014copy number loss2-0272-002SNP arrayGenotyping19
nssv15654705copy number loss3-0193-000SNP arrayGenotyping19
nssv15657346copy number loss3-0380-002SNP arrayGenotyping28
nssv15659717copy number loss4-0070-003SNP arrayGenotyping24
nssv15659768copy number loss4-0073-001SNP arrayGenotyping22
nssv15659815copy number loss4-0073-003SNP arrayGenotyping21
nssv15665635copy number loss7-0082-003SNP arrayGenotyping15
nssv15668267copy number loss7-0187-003SNP arrayGenotyping31
nssv15670558copy number loss7-0193-003SNP arrayGenotyping16
nssv15670809copy number loss7-0295-003SNP arrayGenotyping24
nssv15673186copy number loss9-0029-002SNP arrayGenotyping19
nssv15673419copy number loss9-0030-002SNP arrayGenotyping24
nssv15673518copy number loss9-0034-002SNP arrayGenotyping27
nssv15676928copy number loss188699SNP arrayGenotyping23
nssv15679458copy number loss227244SNP arrayGenotyping29
nssv15679756copy number loss207275SNP arrayGenotyping20
nssv15680815copy number loss230094SSNP arrayGenotyping18
nssv15686640copy number lossOCD152-SM-1338(188608)SNP arrayGenotyping21
nssv15695669copy number lossOCD92-JW-1312SNP arrayGenotyping14
nssv15696545copy number gain160592SNP arrayGenotyping21
nssv15697556copy number loss240711SNP arrayGenotyping27
nssv15700450copy number loss226749SNP arrayGenotyping22
nssv15701398copy number loss79240SNP arrayGenotyping12
nssv15701596copy number loss224728SNP arrayGenotyping26

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15611681RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15612794RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15613062RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15613495RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15614286RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15615025RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15615405RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15615648RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15616929RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15617286RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15617463RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15618110RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15620810RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15623661RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15624100RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15625935RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15626019RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15626277RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15626899RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15628282RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15628855RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15629270RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15629478RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15629787RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15630204RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15630650RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15630732RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15631550RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15632767RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15633251RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15635255RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15640919RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15642184RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15645014RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15654705RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15657346RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15659717RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15659768RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15659815RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15665635RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15668267RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15670558RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15670809RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15673186RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15673419RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15673518RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15676928RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15679458RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15679756RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15680815RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15686640RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15695669RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15696545RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)dup
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15697556RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15700450RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15701398RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15701596RemappedPerfectNC_000019.10:g.(?_
51628547)_(5165414
9_?)del
GRCh38.p12First PassNC_000019.10Chr1951,628,54751,654,149
nssv15611681Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15612794Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15613062Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15613495Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15614286Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15615025Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15615405Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15615648Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15616929Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15617286Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15617463Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15618110Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15620810Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15623661Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15624100Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15625935Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15626019Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15626277Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15626899Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15628282Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15628855Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15629270Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15629478Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15629787Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15630204Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15630650Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15630732Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15631550Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15632767Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15633251Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15635255Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15640919Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15642184Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15645014Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15654705Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15657346Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15659717Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15659768Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15659815Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15665635Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15668267Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15670558Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
nssv15670809Submitted genomicNC_000019.9:g.(?_5
2131800)_(52157402
_?)del
GRCh37 (hg19)NC_000019.9Chr1952,131,80052,157,402
Showing 100 of 114

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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