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nsv4205161

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:182,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 293 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):6,355,193-6,537,193Question Mark
Overlapping variant regions from other studies: 293 SVs from 20 studies. See in: genome view    
Submitted genomic6,464,359-6,646,359Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4205161RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr126,355,1936,537,193
nsv4205161Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr126,464,3596,646,359

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15951860duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15951860RemappedPerfectNC_000012.12:g.635
5193_6537193dup
GRCh38.p12First PassNC_000012.12Chr126,355,1936,537,193
nssv15951860Submitted genomicNC_000012.11:g.646
4359_6646359dup
GRCh37.p13NC_000012.11Chr126,464,3596,646,359

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv159518604.6e-005121694
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