U.S. flag

An official website of the United States government

nsv6778021

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:75,435

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 297 SVs from 55 studies. See in: genome view    
    Submitted genomic97,119,250-97,194,684Question Mark
    Overlapping variant regions from other studies: 297 SVs from 55 studies. See in: genome view    
    Remapped(Score: Perfect):96,454,954-96,530,388Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6778021Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr597,119,25097,194,684
    nsv6778021RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr596,454,95496,530,388

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18708271duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18708271Submitted genomicNC_000005.10:g.971
    19250_97194684dup
    GRCh38 (hg38)NC_000005.10Chr597,119,25097,194,684
    nssv18708271RemappedPerfectNC_000005.9:g.9645
    4954_96530388dup
    GRCh37.p13First PassNC_000005.9Chr596,454,95496,530,388

    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)
    nssv187082714e-061274834
    Support Center