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nsv6769188

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:378,719

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1313 SVs from 77 studies. See in: genome view    
    Submitted genomic9,225,010-9,603,728Question Mark
    Overlapping variant regions from other studies: 1313 SVs from 77 studies. See in: genome view    
    Remapped(Score: Perfect):9,225,122-9,603,840Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6769188Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr59,225,0109,603,728
    nsv6769188RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr59,225,1229,603,840

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18516858deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18516858Submitted genomicNC_000005.10:g.922
    5010_9603728del
    GRCh38 (hg38)NC_000005.10Chr59,225,0109,603,728
    nssv18516858RemappedPerfectNC_000005.9:g.9225
    122_9603840del
    GRCh37.p13First PassNC_000005.9Chr59,225,1229,603,840

    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)
    nssv185168584e-061276168
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