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nsv2821057

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 499 SVs from 25 studies. See in: genome view    
Submitted genomic9,823,150-9,823,150Question Mark
Overlapping variant regions from other studies: 500 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):9,791,190-9,791,190Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2821057Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX9,823,1509,823,150
nsv2821057RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX9,791,1909,791,190

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13706609insertionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13706609Submitted genomicNC_000023.11:g.982
3150_9823151ins55
GRCh38 (hg38)NC_000023.11ChrX9,823,1509,823,150
nssv13706609RemappedPerfectNC_000023.10:g.979
1190_9791191ins55
GRCh37.p13First PassNC_000023.10ChrX9,791,1909,791,190

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)
nssv137066090.7062434
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