U.S. flag

An official website of the United States government

nsv6737289

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,299

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 30 studies. See in: genome view    
    Submitted genomic194,300,984-194,316,282Question Mark
    Overlapping variant regions from other studies: 146 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):194,018,773-194,034,071Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6737289Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3194,300,984194,316,282
    nsv6737289RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3194,018,773194,034,071

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18676646duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18676646Submitted genomicNC_000003.12:g.194
    300984_194316282du
    p
    GRCh38 (hg38)NC_000003.12Chr3194,300,984194,316,282
    nssv18676646RemappedPerfectNC_000003.11:g.194
    018773_194034071du
    p
    GRCh37.p13First PassNC_000003.11Chr3194,018,773194,034,071

    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)
    nssv186766465.3e-0515275734
    Support Center