nsv5549670

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:492

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 301 SVs from 50 studies. See in: genome view    
Submitted genomic113,025,088-113,025,579Question Mark
Overlapping variant regions from other studies: 301 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):113,679,402-113,679,893Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5549670Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13113,025,088113,025,579
nsv5549670RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13113,679,402113,679,893

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17693785insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17693785Submitted genomicNC_000013.11:g.113
025088_113025579in
s640
GRCh38 (hg38)NC_000013.11Chr13113,025,088113,025,579
nssv17693785RemappedPerfectNC_000013.10:g.113
679402_113679893in
s640
GRCh37.p13First PassNC_000013.10Chr13113,679,402113,679,893

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)
nssv176937850.42621685090
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