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nsv5564052

  • 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: 138 SVs from 24 studies. See in: genome view    
Submitted genomic72,899,395-72,899,446Question Mark
Overlapping variant regions from other studies: 138 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):73,191,736-73,191,787Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5564052Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1572,899,39572,899,446
nsv5564052RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1573,191,73673,191,787

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17702453line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17702453Submitted genomicNC_000015.10:g.728
99395_72899446ins6
019
GRCh38 (hg38)NC_000015.10Chr1572,899,39572,899,446
nssv17702453RemappedPerfectNC_000015.9:g.7319
1736_73191787ins60
19
GRCh37.p13First PassNC_000015.9Chr1573,191,73673,191,787

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)
nssv17702453<0.00126402
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