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nsv4195592

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:129,819

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 66 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):61,725,871-61,855,689Question Mark
Overlapping variant regions from other studies: 66 SVs from 15 studies. See in: genome view    
Submitted genomic61,493,343-61,623,161Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4195592RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1161,725,87161,855,689
nsv4195592Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1161,493,34361,623,161

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15951028duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15951028RemappedPerfectNC_000011.10:g.617
25871_61855689dup
GRCh38.p12First PassNC_000011.10Chr1161,725,87161,855,689
nssv15951028Submitted genomicNC_000011.9:g.6149
3343_61623161dup
GRCh37.p13NC_000011.9Chr1161,493,34361,623,161

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)
nssv159510284.6e-005121694
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