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nsv569810

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,581

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 148 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):69,214,001-69,228,581Question Mark
Overlapping variant regions from other studies: 148 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):69,506,340-69,520,920Question Mark
Overlapping variant regions from other studies: 41 SVs from 12 studies. See in: genome view    
Submitted genomic67,293,394-67,307,974Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv569810RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1569,214,00169,228,581
nsv569810RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1569,506,34069,520,920
nsv569810Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000015.8Chr1567,293,39467,307,974

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv844369copy number gainSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv844369RemappedPerfectNC_000015.10:g.(?_
69214001)_(6922858
1_?)dup
GRCh38.p12First PassNC_000015.10Chr1569,214,00169,228,581
nssv844369RemappedPerfectNC_000015.9:g.(?_6
9506340)_(69520920
_?)dup
GRCh37.p13First PassNC_000015.9Chr1569,506,34069,520,920
nssv844369Submitted genomicNC_000015.8:g.(?_6
7293394)_(67307974
_?)dup
NCBI36 (hg18)NC_000015.8Chr1567,293,39467,307,974

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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