U.S. flag

An official website of the United States government

nsv6985415

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:133,518

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 517 SVs from 46 studies. See in: genome view    
    Submitted genomic50,743,521-50,877,038Question Mark
    Overlapping variant regions from other studies: 516 SVs from 46 studies. See in: genome view    
    Remapped(Score: Perfect):48,820,882-48,954,399Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6985415Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1750,743,52150,877,038
    nsv6985415RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1748,820,88248,954,399

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18626702duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18626702Submitted genomicNC_000017.11:g.507
    43521_50877038dup
    GRCh38 (hg38)NC_000017.11Chr1750,743,52150,877,038
    nssv18626702RemappedPerfectNC_000017.10:g.488
    20882_48954399dup
    GRCh37.p13First PassNC_000017.10Chr1748,820,88248,954,399

    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)
    nssv186267024e-061275816
    Support Center