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nsv5558462

  • 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: 125 SVs from 23 studies. See in: genome view    
Submitted genomic69,330,683-69,330,734Question Mark
Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):71,945,599-71,945,650Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5558462Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr969,330,68369,330,734
nsv5558462RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr971,945,59971,945,650

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17023217line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17023217Submitted genomicNC_000009.12:g.693
30683_69330734ins6
018
GRCh38 (hg38)NC_000009.12Chr969,330,68369,330,734
nssv17023217RemappedPerfectNC_000009.11:g.719
45599_71945650ins6
018
GRCh37.p13First PassNC_000009.11Chr971,945,59971,945,650

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)
nssv17023217<0.00146404
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