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nsv6388438

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:501

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 117 SVs from 26 studies. See in: genome view    
    Submitted genomic70,830,587-70,831,087Question Mark
    Overlapping variant regions from other studies: 117 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):71,696,304-71,696,804Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6388438Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr470,830,58770,831,087
    nsv6388438RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr471,696,30471,696,804

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18119137deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18119137Submitted genomicNC_000004.12:g.708
    30587_70831087del
    GRCh38 (hg38)NC_000004.12Chr470,830,58770,831,087
    nssv18119137RemappedPerfectNC_000004.11:g.716
    96304_71696804del
    GRCh37.p13First PassNC_000004.11Chr471,696,30471,696,804

    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)
    nssv18119137<0.001435172
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