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nsv5421166

  • 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: 83 SVs from 21 studies. See in: genome view    
Submitted genomic81,491,944-81,491,995Question Mark
Overlapping variant regions from other studies: 83 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):81,958,288-81,958,339Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5421166Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1481,491,94481,491,995
nsv5421166RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1481,958,28881,958,339

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17699037alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17699037Submitted genomicNC_000014.9:g.8149
1944_81491995ins28
1
GRCh38 (hg38)NC_000014.9Chr1481,491,94481,491,995
nssv17699037RemappedPerfectNC_000014.8:g.8195
8288_81958339ins28
1
GRCh37.p13First PassNC_000014.8Chr1481,958,28881,958,339

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)
nssv176990370.003216404
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