U.S. flag

An official website of the United States government

nsv6999983

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49,237

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 383 SVs from 53 studies. See in: genome view    
    Submitted genomic48,796,658-48,845,894Question Mark
    Overlapping variant regions from other studies: 383 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):49,299,915-49,349,151Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6999983Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,796,65848,845,894
    nsv6999983RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,299,91549,349,151

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18640899duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18640899Submitted genomicNC_000019.10:g.487
    96658_48845894dup
    GRCh38 (hg38)NC_000019.10Chr1948,796,65848,845,894
    nssv18640899RemappedPerfectNC_000019.9:g.4929
    9915_49349151dup
    GRCh37.p13First PassNC_000019.9Chr1949,299,91549,349,151

    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)
    nssv186408997e-062275092
    Support Center