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nsv6320799

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:130

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 118 SVs from 19 studies. See in: genome view    
    Submitted genomic155,918,602-155,918,731Question Mark
    Overlapping variant regions from other studies: 125 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):155,888,393-155,888,522Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6320799Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1155,918,602155,918,731
    nsv6320799RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1155,888,393155,888,522

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18052106deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18052106Submitted genomicNC_000001.11:g.155
    918602_155918731de
    l
    GRCh38 (hg38)NC_000001.11Chr1155,918,602155,918,731
    nssv18052106RemappedPerfectNC_000001.10:g.155
    888393_155888522de
    l
    GRCh37.p13First PassNC_000001.10Chr1155,888,393155,888,522

    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)
    nssv18052106<0.001131838
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