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nsv6501028

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,574

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 85 SVs from 19 studies. See in: genome view    
    Submitted genomic27,881,264-27,883,837Question Mark
    Overlapping variant regions from other studies: 85 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):26,208,290-26,210,863Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6501028Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1727,881,26427,883,837
    nsv6501028RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1726,208,29026,210,863

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18034534deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18034534Submitted genomicNC_000017.11:g.278
    81264_27883837del
    GRCh38 (hg38)NC_000017.11Chr1727,881,26427,883,837
    nssv18034534RemappedPerfectNC_000017.10:g.262
    08290_26210863del
    GRCh37.p13First PassNC_000017.10Chr1726,208,29026,210,863

    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)
    nssv18034534<0.001239162
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