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nsv4924251

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,204

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 32 studies. See in: genome view    
Submitted genomic23,190,590-23,203,793Question Mark
Overlapping variant regions from other studies: 120 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):23,232,081-23,245,284Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4924251Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr323,190,59023,203,793
nsv4924251RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr323,232,08123,245,284

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16453267duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16453267Submitted genomicNC_000003.12:g.231
90590_23203793dup
GRCh38 (hg38)NC_000003.12Chr323,190,59023,203,793
nssv16453267RemappedPerfectNC_000003.11:g.232
32081_23245284dup
GRCh37.p13First PassNC_000003.11Chr323,232,08123,245,284

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16453267<0.001229246
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