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nsv6985927

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,348

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
    Submitted genomic62,700,877-62,708,224Question Mark
    Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):60,778,238-60,785,585Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6985927Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1762,700,87762,708,224
    nsv6985927RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1760,778,23860,785,585

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18411984deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18411984Submitted genomicNC_000017.11:g.627
    00877_62708224del
    GRCh38 (hg38)NC_000017.11Chr1762,700,87762,708,224
    nssv18411984RemappedPerfectNC_000017.10:g.607
    78238_60785585del
    GRCh37.p13First PassNC_000017.10Chr1760,778,23860,785,585

    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)
    nssv184119843.5e-0510276154
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