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nsv6147252

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,439

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 158 SVs from 44 studies. See in: genome view    
Submitted genomic86,101,085-86,110,523Question Mark
Overlapping variant regions from other studies: 158 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):86,567,429-86,576,867Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147252Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1486,101,08586,110,523
nsv6147252RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1486,567,42986,576,867

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17696089mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17696089Submitted genomicNC_000014.9:g.8610
1085_86110523del
GRCh38 (hg38)NC_000014.9Chr1486,101,08586,110,523
nssv17696089RemappedPerfectNC_000014.8:g.8656
7429_86576867del
GRCh37.p13First PassNC_000014.8Chr1486,567,42986,576,867

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)
nssv17696089<0.00116404
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