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nsv6645056

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:355

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 175 SVs from 25 studies. See in: genome view    
    Submitted genomic174,001,363-174,001,717Question Mark
    Overlapping variant regions from other studies: 178 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):173,970,501-173,970,855Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6645056Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1174,001,363174,001,717
    nsv6645056RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1173,970,501173,970,855

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18586390duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18586390Submitted genomicNC_000001.11:g.174
    001363_174001717du
    p
    GRCh38 (hg38)NC_000001.11Chr1174,001,363174,001,717
    nssv18586390RemappedPerfectNC_000001.10:g.173
    970501_173970855du
    p
    GRCh37.p13First PassNC_000001.10Chr1173,970,501173,970,855

    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)
    nssv185863904e-061243132
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