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nsv5553002

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 77 SVs from 21 studies. See in: genome view    
Submitted genomic124,670,518-124,670,526Question Mark
Overlapping variant regions from other studies: 77 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):127,432,797-127,432,805Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5553002Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9124,670,518124,670,526
nsv5553002RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9127,432,797127,432,805

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028634insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028634Submitted genomicNC_000009.12:g.124
670518_124670526in
s119
GRCh38 (hg38)NC_000009.12Chr9124,670,518124,670,526
nssv17028634RemappedPerfectNC_000009.11:g.127
432797_127432805in
s119
GRCh37.p13First PassNC_000009.11Chr9127,432,797127,432,805

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)
nssv170286340.031906404
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