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nsv5399623

  • 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: 67 SVs from 22 studies. See in: genome view    
Submitted genomic8,051,349-8,051,400Question Mark
Overlapping variant regions from other studies: 67 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):8,072,896-8,072,947Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5399623Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr118,051,3498,051,400
nsv5399623RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr118,072,8968,072,947

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17041832alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17041832Submitted genomicNC_000011.10:g.805
1349_8051400ins155
GRCh38 (hg38)NC_000011.10Chr118,051,3498,051,400
nssv17041832RemappedPerfectNC_000011.9:g.8072
896_8072947ins155
GRCh37.p13First PassNC_000011.9Chr118,072,8968,072,947

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)
nssv17041832<0.00126404
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