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nsv4524480

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64,002

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87 SVs from 14 studies. See in: genome view    
Remapped(Score: Perfect):63,343,621-63,407,622Question Mark
Overlapping variant regions from other studies: 95 SVs from 14 studies. See in: genome view    
Submitted genomic62,803,999-62,868,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4524480RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr763,343,62163,407,622
nsv4524480Submitted genomicGRCh37.p13Primary AssemblyNC_000007.13Chr762,803,99962,868,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15980543duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15980543RemappedPerfectNC_000007.14:g.633
43621_63407622dup
GRCh38.p12First PassNC_000007.14Chr763,343,62163,407,622
nssv15980543Submitted genomicNC_000007.13:g.628
03999_62868000dup
GRCh37.p13NC_000007.13Chr762,803,99962,868,000

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)
nssv15980543<0.0011821694
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