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nsv603907

  • Variant Calls:17
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58,389

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2348 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):78,265,373-78,323,761Question Mark
Overlapping variant regions from other studies: 2348 SVs from 95 studies. See in: genome view    
Remapped(Score: Perfect):78,975,090-79,033,478Question Mark
Overlapping variant regions from other studies: 1049 SVs from 32 studies. See in: genome view    
Submitted genomic79,031,809-79,090,197Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv603907RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr678,265,37378,323,761
nsv603907RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr678,975,09079,033,478
nsv603907Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr679,031,80979,090,197

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1066709copy number lossSNP arraySNP genotyping analysis
nssv1066710copy number lossSNP arraySNP genotyping analysis
nssv1066711copy number lossSNP arraySNP genotyping analysis
nssv1066712copy number lossSNP arraySNP genotyping analysis
nssv1066713copy number lossSNP arraySNP genotyping analysis
nssv1066714copy number lossSNP arraySNP genotyping analysis
nssv1066715copy number lossSNP arraySNP genotyping analysis
nssv1066716copy number gainSNP arraySNP genotyping analysis
nssv1066717copy number lossSNP arraySNP genotyping analysis
nssv1066718copy number lossSNP arraySNP genotyping analysis
nssv1066719copy number gainSNP arraySNP genotyping analysis
nssv1066720copy number lossSNP arraySNP genotyping analysis
nssv1066721copy number gainSNP arraySNP genotyping analysis
nssv1066722copy number lossSNP arraySNP genotyping analysis
nssv1066723copy number lossSNP arraySNP genotyping analysis
nssv1066724copy number lossSNP arraySNP genotyping analysis
nssv1066725copy number lossSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1066709RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066710RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066711RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066712RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066713RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066714RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066715RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066716RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)dup
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066717RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066718RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066719RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)dup
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066720RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066721RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)dup
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066722RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066723RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066724RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066725RemappedPerfectNC_000006.12:g.(?_
78265373)_(7832376
1_?)del
GRCh38.p12First PassNC_000006.12Chr678,265,37378,323,761
nssv1066709RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066710RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066711RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066712RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066713RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066714RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066715RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066716RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)dup
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066717RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066718RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066719RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)dup
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066720RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066721RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)dup
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066722RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066723RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066724RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066725RemappedPerfectNC_000006.11:g.(?_
78975090)_(7903347
8_?)del
GRCh37.p13First PassNC_000006.11Chr678,975,09079,033,478
nssv1066709Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066710Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066711Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066712Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066713Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066714Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066715Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066716Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)dup
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066717Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066718Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066719Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)dup
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066720Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066721Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)dup
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066722Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066723Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066724Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197
nssv1066725Submitted genomicNC_000006.10:g.(?_
79031809)_(7909019
7_?)del
NCBI36 (hg18)NC_000006.10Chr679,031,80979,090,197

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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