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nsv5417173

  • 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: 75 SVs from 18 studies. See in: genome view    
Submitted genomic81,473,182-81,473,233Question Mark
Overlapping variant regions from other studies: 75 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):81,939,526-81,939,577Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5417173Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1481,473,18281,473,233
nsv5417173RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1481,939,52681,939,577

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17699036alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17699036Submitted genomicNC_000014.9:g.8147
3182_81473233ins27
9
GRCh38 (hg38)NC_000014.9Chr1481,473,18281,473,233
nssv17699036RemappedPerfectNC_000014.8:g.8193
9526_81939577ins27
9
GRCh37.p13First PassNC_000014.8Chr1481,939,52681,939,577

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)
nssv17699036<0.00116404
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