U.S. flag

An official website of the United States government

nsv6665374

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:154,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 500 SVs from 59 studies. See in: genome view    
    Submitted genomic192,506,601-192,661,100Question Mark
    Overlapping variant regions from other studies: 500 SVs from 59 studies. See in: genome view    
    Remapped(Score: Perfect):192,475,731-192,630,230Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6665374Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1192,506,601192,661,100
    nsv6665374RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1192,475,731192,630,230

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18366032deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18366032Submitted genomicNC_000001.11:g.192
    506601_192661100de
    l
    GRCh38 (hg38)NC_000001.11Chr1192,506,601192,661,100
    nssv18366032RemappedPerfectNC_000001.10:g.192
    475731_192630230de
    l
    GRCh37.p13First PassNC_000001.10Chr1192,475,731192,630,230

    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)
    nssv183660321.2e-053250572
    Support Center