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nsv5480308

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:638

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 34 studies. See in: genome view    
Submitted genomic129,642,484-129,643,121Question Mark
Overlapping variant regions from other studies: 153 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):132,404,763-132,405,400Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5480308Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9129,642,484129,643,121
nsv5480308RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9132,404,763132,405,400

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028109deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028109Submitted genomicNC_000009.12:g.129
642484_129643121de
l
GRCh38 (hg38)NC_000009.12Chr9129,642,484129,643,121
nssv17028109RemappedPerfectNC_000009.11:g.132
404763_132405400de
l
GRCh37.p13First PassNC_000009.11Chr9132,404,763132,405,400

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)
nssv170281090.003186404
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