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nsv5563770

  • 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: 98 SVs from 18 studies. See in: genome view    
Submitted genomic79,805,618-79,805,669Question Mark
Overlapping variant regions from other studies: 98 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):80,032,744-80,032,795Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563770Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr279,805,61879,805,669
nsv5563770RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr280,032,74480,032,795

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16915781sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16915781Submitted genomicNC_000002.12:g.798
05618_79805669ins1
316
GRCh38 (hg38)NC_000002.12Chr279,805,61879,805,669
nssv16915781RemappedPerfectNC_000002.11:g.800
32744_80032795ins1
316
GRCh37.p13First PassNC_000002.11Chr280,032,74480,032,795

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)
nssv16915781<0.00136402
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