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nsv6642739

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,828

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view    
    Submitted genomic155,869,870-155,872,697Question Mark
    Overlapping variant regions from other studies: 126 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):155,839,661-155,842,488Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6642739Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1155,869,870155,872,697
    nsv6642739RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1155,839,661155,842,488

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18362288deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18362288Submitted genomicNC_000001.11:g.155
    869870_155872697de
    l
    GRCh38 (hg38)NC_000001.11Chr1155,869,870155,872,697
    nssv18362288RemappedPerfectNC_000001.10:g.155
    839661_155842488de
    l
    GRCh37.p13First PassNC_000001.10Chr1155,839,661155,842,488

    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)
    nssv183622884e-061275940
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