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nsv6147499

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,674

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 301 SVs from 70 studies. See in: genome view    
Submitted genomic41,235,484-41,247,157Question Mark
Overlapping variant regions from other studies: 299 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):39,391,736-39,403,409Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147499Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1741,235,48441,247,157
nsv6147499RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1739,391,73639,403,409

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713173mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713173Submitted genomicNC_000017.11:g.412
35484_41247157del
GRCh38 (hg38)NC_000017.11Chr1741,235,48441,247,157
nssv17713173RemappedPerfectNC_000017.10:g.393
91736_39403409del
GRCh37.p13First PassNC_000017.10Chr1739,391,73639,403,409

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)
nssv177131730.002116404
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