U.S. flag

An official website of the United States government

nsv7072532

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,638

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 102 SVs from 30 studies. See in: genome view    
    Submitted genomic52,544,701-52,547,338Question Mark
    Overlapping variant regions from other studies: 102 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):53,047,954-53,050,591Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7072532Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1952,544,70152,547,338
    nsv7072532RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1953,047,95453,050,591

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18760666inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18760666Submitted genomicNC_000019.10:g.525
    44701_52547338inv
    GRCh38 (hg38)NC_000019.10Chr1952,544,70152,547,338
    nssv18760666RemappedPerfectNC_000019.9:g.5304
    7954_53050591inv
    GRCh37.p13First PassNC_000019.9Chr1953,047,95453,050,591

    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)
    nssv187606661.1e-053274154
    Support Center