U.S. flag

An official website of the United States government

nsv6728082

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,069

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 240 SVs from 34 studies. See in: genome view    
    Submitted genomic4,283,620-4,294,688Question Mark
    Overlapping variant regions from other studies: 240 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):4,285,347-4,296,415Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6728082Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr44,283,6204,294,688
    nsv6728082RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr44,285,3474,296,415

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18494687deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18494687Submitted genomicNC_000004.12:g.428
    3620_4294688del
    GRCh38 (hg38)NC_000004.12Chr44,283,6204,294,688
    nssv18494687RemappedPerfectNC_000004.11:g.428
    5347_4296415del
    GRCh37.p13First PassNC_000004.11Chr44,285,3474,296,415

    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)
    nssv184946877e-062276262
    Support Center