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nsv4191998

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,382

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 52 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):5,423,420-5,424,801Question Mark
Overlapping variant regions from other studies: 52 SVs from 8 studies. See in: genome view    
Submitted genomic5,465,383-5,466,764Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4191998RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr105,423,4205,424,801
nsv4191998Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr105,465,3835,466,764

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15792212deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15792212RemappedPerfectNC_000010.11:g.542
3420_5424801del
GRCh38.p12First PassNC_000010.11Chr105,423,4205,424,801
nssv15792212Submitted genomicNC_000010.10:g.546
5383_5466764del
GRCh37.p13NC_000010.10Chr105,465,3835,466,764

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)
nssv15792212<0.001721694
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