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nsv4210577

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,433

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 74 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):6,866,688-6,873,120Question Mark
Overlapping variant regions from other studies: 72 SVs from 6 studies. See in: genome view    
Submitted genomic6,975,852-6,982,284Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4210577RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr126,866,6886,873,120
nsv4210577Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr126,975,8526,982,284

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15806278deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15806278RemappedPerfectNC_000012.12:g.686
6688_6873120del
GRCh38.p12First PassNC_000012.12Chr126,866,6886,873,120
nssv15806278Submitted genomicNC_000012.11:g.697
5852_6982284del
GRCh37.p13NC_000012.11Chr126,975,8526,982,284

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)
nssv158062789.2e-005221690
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