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nsv5487254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,208

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 36 studies. See in: genome view    
Submitted genomic113,156,532-113,160,739Question Mark
Overlapping variant regions from other studies: 124 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):115,918,812-115,923,019Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9113,156,532113,160,739
nsv5487254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9115,918,812115,923,019

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17026364deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17026364Submitted genomicNC_000009.12:g.113
156532_113160739de
l
GRCh38 (hg38)NC_000009.12Chr9113,156,532113,160,739
nssv17026364RemappedPerfectNC_000009.11:g.115
918812_115923019de
l
GRCh37.p13First PassNC_000009.11Chr9115,918,812115,923,019

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)
nssv17026364<0.00116404
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