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nsv6772948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 200 SVs from 32 studies. See in: genome view    
    Submitted genomic112,127,101-112,161,000Question Mark
    Overlapping variant regions from other studies: 200 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):111,462,798-111,496,697Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6772948Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5112,127,101112,161,000
    nsv6772948RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5111,462,798111,496,697

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18506188deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18506188Submitted genomicNC_000005.10:g.112
    127101_112161000de
    l
    GRCh38 (hg38)NC_000005.10Chr5112,127,101112,161,000
    nssv18506188RemappedPerfectNC_000005.9:g.1114
    62798_111496697del
    GRCh37.p13First PassNC_000005.9Chr5111,462,798111,496,697

    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)
    nssv185061884e-061276204
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