U.S. flag

An official website of the United States government

nsv6921941

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,717

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 133 SVs from 37 studies. See in: genome view    
    Submitted genomic75,351,587-75,362,303Question Mark
    Overlapping variant regions from other studies: 133 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):75,745,367-75,756,083Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6921941Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1275,351,58775,362,303
    nsv6921941RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1275,745,36775,756,083

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18371987deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18371987Submitted genomicNC_000012.12:g.753
    51587_75362303del
    GRCh38 (hg38)NC_000012.12Chr1275,351,58775,362,303
    nssv18371987RemappedPerfectNC_000012.11:g.757
    45367_75756083del
    GRCh37.p13First PassNC_000012.11Chr1275,745,36775,756,083

    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)
    nssv183719875e-0514276128
    Support Center