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nsv6750752

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,448

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 168 SVs from 35 studies. See in: genome view    
    Submitted genomic75,862,020-75,875,467Question Mark
    Overlapping variant regions from other studies: 168 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):76,783,173-76,796,620Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6750752Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr475,862,02075,875,467
    nsv6750752RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr476,783,17376,796,620

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18501071deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18501071Submitted genomicNC_000004.12:g.758
    62020_75875467del
    GRCh38 (hg38)NC_000004.12Chr475,862,02075,875,467
    nssv18501071RemappedPerfectNC_000004.11:g.767
    83173_76796620del
    GRCh37.p13First PassNC_000004.11Chr476,783,17376,796,620

    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)
    nssv18501071<0.00126276004
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