U.S. flag

An official website of the United States government

nsv6720928

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:122,603

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 437 SVs from 54 studies. See in: genome view    
    Submitted genomic191,157,483-191,280,085Question Mark
    Overlapping variant regions from other studies: 437 SVs from 54 studies. See in: genome view    
    Remapped(Score: Perfect):190,875,272-190,997,874Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6720928Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3191,157,483191,280,085
    nsv6720928RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3190,875,272190,997,874

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18477648deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18477648Submitted genomicNC_000003.12:g.191
    157483_191280085de
    l
    GRCh38 (hg38)NC_000003.12Chr3191,157,483191,280,085
    nssv18477648RemappedPerfectNC_000003.11:g.190
    875272_190997874de
    l
    GRCh37.p13First PassNC_000003.11Chr3190,875,272190,997,874

    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)
    nssv184776481.1e-053276230
    Support Center