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nsv6608742

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:986

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 22 studies. See in: genome view    
    Submitted genomic116,865,433-116,866,418Question Mark
    Overlapping variant regions from other studies: 109 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):116,505,487-116,506,472Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6608742Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7116,865,433116,866,418
    nsv6608742RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7116,505,487116,506,472

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18217953duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18217953Submitted genomicNC_000007.14:g.116
    865433_116866418du
    p
    GRCh38 (hg38)NC_000007.14Chr7116,865,433116,866,418
    nssv18217953RemappedPerfectNC_000007.13:g.116
    505487_116506472du
    p
    GRCh37.p13First PassNC_000007.13Chr7116,505,487116,506,472

    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)
    nssv18217953<0.001339036
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