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nsv6776333

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,497

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 23 studies. See in: genome view    
    Submitted genomic112,415,252-112,424,748Question Mark
    Overlapping variant regions from other studies: 146 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):111,750,949-111,760,445Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6776333Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5112,415,252112,424,748
    nsv6776333RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5111,750,949111,760,445

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18506219deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18506219Submitted genomicNC_000005.10:g.112
    415252_112424748de
    l
    GRCh38 (hg38)NC_000005.10Chr5112,415,252112,424,748
    nssv18506219RemappedPerfectNC_000005.9:g.1117
    50949_111760445del
    GRCh37.p13First PassNC_000005.9Chr5111,750,949111,760,445

    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)
    nssv185062194e-061276236
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