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nsv5562924

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 110 SVs from 20 studies. See in: genome view    
Submitted genomic92,237,947-92,237,998Question Mark
Overlapping variant regions from other studies: 110 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):92,703,504-92,703,555Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5562924Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr192,237,94792,237,998
nsv5562924RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr192,703,50492,703,555

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16906465line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16906465Submitted genomicNC_000001.11:g.922
37947_92237998ins6
016
GRCh38 (hg38)NC_000001.11Chr192,237,94792,237,998
nssv16906465RemappedPerfectNC_000001.10:g.927
03504_92703555ins6
016
GRCh37.p13First PassNC_000001.10Chr192,703,50492,703,555

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)
nssv16906465<0.00116404
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