U.S. flag

An official website of the United States government

nsv7006150

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:124,978

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 735 SVs from 61 studies. See in: genome view    
    Submitted genomic76,144,583-76,269,560Question Mark
    Overlapping variant regions from other studies: 735 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):73,856,538-73,981,515Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7006150Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1876,144,58376,269,560
    nsv7006150RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1873,856,53873,981,515

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18635027duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18635027Submitted genomicNC_000018.10:g.761
    44583_76269560dup
    GRCh38 (hg38)NC_000018.10Chr1876,144,58376,269,560
    nssv18635027RemappedPerfectNC_000018.9:g.7385
    6538_73981515dup
    GRCh37.p13First PassNC_000018.9Chr1873,856,53873,981,515

    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)
    nssv186350274e-061275496
    Support Center