U.S. flag

An official website of the United States government

nsv6995769

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:174,762

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 552 SVs from 56 studies. See in: genome view    
    Submitted genomic12,884,733-13,059,494Question Mark
    Overlapping variant regions from other studies: 552 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):12,788,050-12,962,811Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6995769Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1712,884,73313,059,494
    nsv6995769RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1712,788,05012,962,811

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626223duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626223Submitted genomicNC_000017.11:g.128
    84733_13059494dup
    GRCh38 (hg38)NC_000017.11Chr1712,884,73313,059,494
    nssv18626223RemappedPerfectNC_000017.10:g.127
    88050_12962811dup
    GRCh37.p13First PassNC_000017.10Chr1712,788,05012,962,811

    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)
    nssv186262232.1e-056275294
    Support Center