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nsv5394312

  • 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: 63 SVs from 19 studies. See in: genome view    
Submitted genomic6,581,107-6,581,158Question Mark
Overlapping variant regions from other studies: 63 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):6,602,337-6,602,388Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5394312Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr116,581,1076,581,158
nsv5394312RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr116,602,3376,602,388

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17041704alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17041704Submitted genomicNC_000011.10:g.658
1107_6581158ins261
GRCh38 (hg38)NC_000011.10Chr116,581,1076,581,158
nssv17041704RemappedPerfectNC_000011.9:g.6602
337_6602388ins261
GRCh37.p13First PassNC_000011.9Chr116,602,3376,602,388

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)
nssv17041704<0.00126404
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