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nsv5926948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 173 SVs from 35 studies. See in: genome view    
Submitted genomic129,340,788-129,340,861Question Mark
Overlapping variant regions from other studies: 173 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):132,103,067-132,103,140Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5926948Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9129,340,788129,340,861
nsv5926948RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9132,103,067132,103,140

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17439516deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17439516Submitted genomicNC_000009.12:g.129
340788_129340861de
l
GRCh38 (hg38)NC_000009.12Chr9129,340,788129,340,861
nssv17439516RemappedPerfectNC_000009.11:g.132
103067_132103140de
l
GRCh37.p13First PassNC_000009.11Chr9132,103,067132,103,140

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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