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nsv889773

  • Variant Calls:3
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85,546

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1393 SVs from 97 studies. See in: genome view    
Remapped(Score: Good):2,182,989-2,268,534Question Mark
Overlapping variant regions from other studies: 811 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):366,396-449,523Question Mark
Overlapping variant regions from other studies: 1017 SVs from 91 studies. See in: genome view    
Remapped(Score: Perfect):2,131,186-2,214,313Question Mark
Overlapping variant regions from other studies: 805 SVs from 56 studies. See in: genome view    
Remapped(Score: Perfect):165,797-248,924Question Mark
Overlapping variant regions from other studies: 504 SVs from 29 studies. See in: genome view    
Submitted genomic2,118,593-2,201,720Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv889773RemappedGoodGRCh38.p12Primary AssemblySecond PassNC_000008.11Chr82,182,9892,182,9892,268,5342,268,534
nsv889773RemappedPerfectGRCh38.p12ALT_REF_LOCI_1First PassNT_187576.1Chr8|NT_18
7576.1		366,396368,548448,153449,523
nsv889773RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000008.10Chr82,131,1862,133,3382,212,9432,214,313
nsv889773RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003571042.1Chr8|NW_00
3571042.1		165,797167,949247,554248,924
nsv889773Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000008.9Chr82,118,5932,120,7452,200,3502,201,720

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1521967copy number gainSP52680SNP arraySNP genotyping analysis9
nssv1526240copy number gainSP57137SNP arraySNP genotyping analysis12
nssv1528743copy number gainSP81354SNP arraySNP genotyping analysis16

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1521967RemappedPerfectNT_187576.1:g.(366
396_368548)_(44815
3_449523)dup		GRCh38.p12First PassNT_187576.1Chr8|NT_18
7576.1		366,396368,548448,153449,523
nssv1526240RemappedPerfectNT_187576.1:g.(366
396_368548)_(44815
3_449523)dup		GRCh38.p12First PassNT_187576.1Chr8|NT_18
7576.1		366,396368,548448,153449,523
nssv1528743RemappedPerfectNT_187576.1:g.(366
396_368548)_(44815
3_449523)dup		GRCh38.p12First PassNT_187576.1Chr8|NT_18
7576.1		366,396368,548448,153449,523
nssv1521967RemappedGoodNC_000008.11:g.(21
82989_2182989)_(22
68534_2268534)dup		GRCh38.p12Second PassNC_000008.11Chr82,182,9892,182,9892,268,5342,268,534
nssv1526240RemappedGoodNC_000008.11:g.(21
82989_2182989)_(22
68534_2268534)dup		GRCh38.p12Second PassNC_000008.11Chr82,182,9892,182,9892,268,5342,268,534
nssv1528743RemappedGoodNC_000008.11:g.(21
82989_2182989)_(22
68534_2268534)dup		GRCh38.p12Second PassNC_000008.11Chr82,182,9892,182,9892,268,5342,268,534
nssv1521967RemappedPerfectNW_003571042.1:g.(
165797_167949)_(24
7554_248924)dup		GRCh37.p13First PassNW_003571042.1Chr8|NW_00
3571042.1		165,797167,949247,554248,924
nssv1526240RemappedPerfectNW_003571042.1:g.(
165797_167949)_(24
7554_248924)dup		GRCh37.p13First PassNW_003571042.1Chr8|NW_00
3571042.1		165,797167,949247,554248,924
nssv1528743RemappedPerfectNW_003571042.1:g.(
165797_167949)_(24
7554_248924)dup		GRCh37.p13First PassNW_003571042.1Chr8|NW_00
3571042.1		165,797167,949247,554248,924
nssv1521967RemappedPerfectNC_000008.10:g.(21
31186_2133338)_(22
12943_2214313)dup		GRCh37.p13Second PassNC_000008.10Chr82,131,1862,133,3382,212,9432,214,313
nssv1526240RemappedPerfectNC_000008.10:g.(21
31186_2133338)_(22
12943_2214313)dup		GRCh37.p13Second PassNC_000008.10Chr82,131,1862,133,3382,212,9432,214,313
nssv1528743RemappedPerfectNC_000008.10:g.(21
31186_2133338)_(22
12943_2214313)dup		GRCh37.p13Second PassNC_000008.10Chr82,131,1862,133,3382,212,9432,214,313
nssv1521967Submitted genomicNC_000008.9:g.(211
8593_2120745)_(220
0350_2201720)dup		NCBI36 (hg18)NC_000008.9Chr82,118,5932,120,7452,200,3502,201,720
nssv1526240Submitted genomicNC_000008.9:g.(211
8593_2120745)_(220
0350_2201720)dup		NCBI36 (hg18)NC_000008.9Chr82,118,5932,120,7452,200,3502,201,720
nssv1528743Submitted genomicNC_000008.9:g.(211
8593_2120745)_(220
0350_2201720)dup		NCBI36 (hg18)NC_000008.9Chr82,118,5932,120,7452,200,3502,201,720

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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