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nsv437973

  • Variant Calls:22
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,472

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2474 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):78,290,181-78,322,652Question Mark
Overlapping variant regions from other studies: 2474 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):78,999,898-79,032,369Question Mark
Overlapping variant regions from other studies: 9 SVs from 1 studies. See in: genome view    
Submitted genomic78,995,494-79,027,965Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv437973RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr678,290,18178,322,652
nsv437973RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr678,999,89879,032,369
nsv437973Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000006.8Chr678,995,49479,027,965

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv468805copy number lossNA18862SNP arraySNP genotyping analysis12
nssv468806copy number lossNA18863SNP arraySNP genotyping analysis16
nssv468808copy number lossNA18913SNP arraySNP genotyping analysis15
nssv468809copy number lossNA18914SNP arraySNP genotyping analysis26
nssv468786copy number lossNA12144SNP arraySNP genotyping analysis17
nssv468787copy number lossNA10846SNP arraySNP genotyping analysis33
nssv468788copy number lossNA12145SNP arraySNP genotyping analysis15
nssv468789copy number lossNA10846SNP arraySNP genotyping analysis33
nssv468790copy number lossNA12003SNP arraySNP genotyping analysis16
nssv468791copy number lossNA10838SNP arraySNP genotyping analysis19
nssv468792copy number lossNA12236SNP arraySNP genotyping analysis9
nssv468793copy number lossNA10830SNP arraySNP genotyping analysis17
nssv468794copy number lossNA06994SNP arraySNP genotyping analysis22
nssv468795copy number lossNA07029SNP arraySNP genotyping analysis25
nssv468797copy number lossNA07022SNP arraySNP genotyping analysis7
nssv468798copy number lossNA07019SNP arraySNP genotyping analysis21
nssv468799copy number lossNA12144SNP arraySNP genotyping analysis17
nssv468800copy number lossNA10846SNP arraySNP genotyping analysis33
nssv468801copy number lossNA12145SNP arraySNP genotyping analysis15
nssv468802copy number lossNA10846SNP arraySNP genotyping analysis33
nssv468803copy number lossNA12249SNP arraySNP genotyping analysis16
nssv468804copy number lossNA10835SNP arraySNP genotyping analysis28

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv468805RemappedPerfectNC_000006.12:g.(?_
78290181)_(7831664
7_?)del
GRCh38.p12First PassNC_000006.12Chr678,290,18178,316,647
nssv468806RemappedPerfectNC_000006.12:g.(?_
78290181)_(7831664
7_?)del
GRCh38.p12First PassNC_000006.12Chr678,290,18178,316,647
nssv468808RemappedPerfectNC_000006.12:g.(?_
78290181)_(7831664
7_?)del
GRCh38.p12First PassNC_000006.12Chr678,290,18178,316,647
nssv468809RemappedPerfectNC_000006.12:g.(?_
78290181)_(7831664
7_?)del
GRCh38.p12First PassNC_000006.12Chr678,290,18178,316,647
nssv468786RemappedPerfectNC_000006.12:g.(?_
78293361)_(7831696
9_?)del
GRCh38.p12First PassNC_000006.12Chr678,293,36178,316,969
nssv468787RemappedPerfectNC_000006.12:g.(?_
78293361)_(7831696
9_?)del
GRCh38.p12First PassNC_000006.12Chr678,293,36178,316,969
nssv468788RemappedPerfectNC_000006.12:g.(?_
78293361)_(7831696
9_?)del
GRCh38.p12First PassNC_000006.12Chr678,293,36178,316,969
nssv468789RemappedPerfectNC_000006.12:g.(?_
78293361)_(7831696
9_?)del
GRCh38.p12First PassNC_000006.12Chr678,293,36178,316,969
nssv468790RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468791RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468792RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468793RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468794RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468795RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468797RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468798RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468799RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468800RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468801RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468802RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468803RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468804RemappedPerfectNC_000006.12:g.(?_
78316647)_(7832265
2_?)del
GRCh38.p12First PassNC_000006.12Chr678,316,64778,322,652
nssv468805RemappedPerfectNC_000006.11:g.(?_
78999898)_(7902636
4_?)del
GRCh37.p13First PassNC_000006.11Chr678,999,89879,026,364
nssv468806RemappedPerfectNC_000006.11:g.(?_
78999898)_(7902636
4_?)del
GRCh37.p13First PassNC_000006.11Chr678,999,89879,026,364
nssv468808RemappedPerfectNC_000006.11:g.(?_
78999898)_(7902636
4_?)del
GRCh37.p13First PassNC_000006.11Chr678,999,89879,026,364
nssv468809RemappedPerfectNC_000006.11:g.(?_
78999898)_(7902636
4_?)del
GRCh37.p13First PassNC_000006.11Chr678,999,89879,026,364
nssv468786RemappedPerfectNC_000006.11:g.(?_
79003078)_(7902668
6_?)del
GRCh37.p13First PassNC_000006.11Chr679,003,07879,026,686
nssv468787RemappedPerfectNC_000006.11:g.(?_
79003078)_(7902668
6_?)del
GRCh37.p13First PassNC_000006.11Chr679,003,07879,026,686
nssv468788RemappedPerfectNC_000006.11:g.(?_
79003078)_(7902668
6_?)del
GRCh37.p13First PassNC_000006.11Chr679,003,07879,026,686
nssv468789RemappedPerfectNC_000006.11:g.(?_
79003078)_(7902668
6_?)del
GRCh37.p13First PassNC_000006.11Chr679,003,07879,026,686
nssv468790RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468791RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468792RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468793RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468794RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468795RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468797RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468798RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468799RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468800RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468801RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468802RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468803RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468804RemappedPerfectNC_000006.11:g.(?_
79026364)_(7903236
9_?)del
GRCh37.p13First PassNC_000006.11Chr679,026,36479,032,369
nssv468805Submitted genomicNC_000006.8:g.(?_7
8995494)_(79021960
_?)del
NCBI34 (hg16)NC_000006.8Chr678,995,49479,021,960
nssv468806Submitted genomicNC_000006.8:g.(?_7
8995494)_(79021960
_?)del
NCBI34 (hg16)NC_000006.8Chr678,995,49479,021,960
nssv468808Submitted genomicNC_000006.8:g.(?_7
8995494)_(79021960
_?)del
NCBI34 (hg16)NC_000006.8Chr678,995,49479,021,960
nssv468809Submitted genomicNC_000006.8:g.(?_7
8995494)_(79021960
_?)del
NCBI34 (hg16)NC_000006.8Chr678,995,49479,021,960
nssv468786Submitted genomicNC_000006.8:g.(?_7
8998674)_(79022282
_?)del
NCBI34 (hg16)NC_000006.8Chr678,998,67479,022,282
nssv468787Submitted genomicNC_000006.8:g.(?_7
8998674)_(79022282
_?)del
NCBI34 (hg16)NC_000006.8Chr678,998,67479,022,282
nssv468788Submitted genomicNC_000006.8:g.(?_7
8998674)_(79022282
_?)del
NCBI34 (hg16)NC_000006.8Chr678,998,67479,022,282
nssv468789Submitted genomicNC_000006.8:g.(?_7
8998674)_(79022282
_?)del
NCBI34 (hg16)NC_000006.8Chr678,998,67479,022,282
nssv468790Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468791Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468792Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468793Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468794Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468795Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468797Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468798Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468799Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468800Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468801Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468802Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468803Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965
nssv468804Submitted genomicNC_000006.8:g.(?_7
9021960)_(79027965
_?)del
NCBI34 (hg16)NC_000006.8Chr679,021,96079,027,965

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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