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nsv5536347

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 112 SVs from 32 studies. See in: genome view    
Submitted genomic113,207,344-113,207,344Question Mark
Overlapping variant regions from other studies: 112 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):115,969,624-115,969,624Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5536347Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9113,207,344113,207,344
nsv5536347RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9115,969,624115,969,624

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17026367insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17026367Submitted genomicNC_000009.12:g.113
207344_113207345in
s313
GRCh38 (hg38)NC_000009.12Chr9113,207,344113,207,344
nssv17026367RemappedPerfectNC_000009.11:g.115
969624_115969625in
s313
GRCh37.p13First PassNC_000009.11Chr9115,969,624115,969,624

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)
nssv170263670.20412636196
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