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nsv948928

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:488,675

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1762 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):6,039,494-6,528,168Question Mark
Overlapping variant regions from other studies: 1762 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):6,089,495-6,578,169Question Mark
Overlapping variant regions from other studies: 87 SVs from 7 studies. See in: genome view    
Submitted genomic6,029,496-6,518,170Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv948928RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr166,039,4946,528,168
nsv948928RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr166,089,4956,578,169
nsv948928Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000016.8Chr166,029,4966,518,170

Variant Call Information

Variant Call IDTypeMethodAnalysisCopy number
nssv2767519copy number lossSNP arraySNP genotyping analysis1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv2767519RemappedPerfectNC_000016.10:g.(?_
6039494)_(6528168_
?)del
GRCh38.p12First PassNC_000016.10Chr166,039,4946,528,168
nssv2767519RemappedPerfectNC_000016.9:g.(?_6
089495)_(6578169_?
)del
GRCh37.p13First PassNC_000016.9Chr166,089,4956,578,169
nssv2767519Submitted genomicNC_000016.8:g.(?_6
029496)_(6518170_?
)del
NCBI35 (hg17)NC_000016.8Chr166,029,4966,518,170

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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