U.S. flag

An official website of the United States government

nsv7045378

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:697,672

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2070 SVs from 107 studies. See in: genome view    
    Submitted genomic107,773,299-108,470,970Question Mark
    Overlapping variant regions from other studies: 2071 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):108,315,921-109,013,592Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7045378Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1107,773,299108,470,970
    nsv7045378RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1108,315,921109,013,592

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18744091inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18744091Submitted genomicNC_000001.11:g.107
    773299_108470970in
    v
    GRCh38 (hg38)NC_000001.11Chr1107,773,299108,470,970
    nssv18744091RemappedPerfectNC_000001.10:g.108
    315921_109013592in
    v
    GRCh37.p13First PassNC_000001.10Chr1108,315,921109,013,592

    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)
    nssv187440914.6e-0513275276
    Support Center