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nsv6787723

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,768

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 72 SVs from 13 studies. See in: genome view    
    Submitted genomic160,361,588-160,365,355Question Mark
    Overlapping variant regions from other studies: 72 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):159,788,595-159,792,362Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6787723Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5160,361,588160,365,355
    nsv6787723RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5159,788,595159,792,362

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18510145deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18510145Submitted genomicNC_000005.10:g.160
    361588_160365355de
    l
    GRCh38 (hg38)NC_000005.10Chr5160,361,588160,365,355
    nssv18510145RemappedPerfectNC_000005.9:g.1597
    88595_159792362del
    GRCh37.p13First PassNC_000005.9Chr5159,788,595159,792,362

    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)
    nssv185101454e-061276184
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