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nsv6884956

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,293

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 73 SVs from 15 studies. See in: genome view    
    Submitted genomic97,872,483-97,876,775Question Mark
    Overlapping variant regions from other studies: 73 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):99,632,240-99,636,532Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6884956Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1097,872,48397,876,775
    nsv6884956RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1099,632,24099,636,532

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18341602deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18341602Submitted genomicNC_000010.11:g.978
    72483_97876775del
    GRCh38 (hg38)NC_000010.11Chr1097,872,48397,876,775
    nssv18341602RemappedPerfectNC_000010.10:g.996
    32240_99636532del
    GRCh37.p13First PassNC_000010.10Chr1099,632,24099,636,532

    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)
    nssv183416024e-061276206
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