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nsv5564020

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 29 studies. See in: genome view    
Submitted genomic131,575,960-131,576,011Question Mark
Overlapping variant regions from other studies: 132 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):134,451,347-134,451,398Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5564020Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9131,575,960131,576,011
nsv5564020RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9134,451,347134,451,398

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17029910sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17029910Submitted genomicNC_000009.12:g.131
575960_131576011in
s799
GRCh38 (hg38)NC_000009.12Chr9131,575,960131,576,011
nssv17029910RemappedPerfectNC_000009.11:g.134
451347_134451398in
s799
GRCh37.p13First PassNC_000009.11Chr9134,451,347134,451,398

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)
nssv17029910<0.00116404
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