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nsv6795715

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48,951

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 177 SVs from 40 studies. See in: genome view    
    Submitted genomic170,470,700-170,519,650Question Mark
    Overlapping variant regions from other studies: 177 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):169,897,704-169,946,654Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6795715Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5170,470,700170,519,650
    nsv6795715RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5169,897,704169,946,654

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18510548deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18510548Submitted genomicNC_000005.10:g.170
    470700_170519650de
    l
    GRCh38 (hg38)NC_000005.10Chr5170,470,700170,519,650
    nssv18510548RemappedPerfectNC_000005.9:g.1698
    97704_169946654del
    GRCh37.p13First PassNC_000005.9Chr5169,897,704169,946,654

    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)
    nssv185105484e-061276228
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