U.S. flag

An official website of the United States government

nsv6839228

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,534

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 150 SVs from 22 studies. See in: genome view    
    Submitted genomic97,451,248-97,460,781Question Mark
    Overlapping variant regions from other studies: 150 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):98,463,476-98,473,009Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6839228Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr897,451,24897,460,781
    nsv6839228RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr898,463,47698,473,009

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18750990duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18750990Submitted genomicNC_000008.11:g.974
    51248_97460781dup
    GRCh38 (hg38)NC_000008.11Chr897,451,24897,460,781
    nssv18750990RemappedPerfectNC_000008.10:g.984
    63476_98473009dup
    GRCh37.p13First PassNC_000008.10Chr898,463,47698,473,009

    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)
    nssv187509904e-061275932
    Support Center