U.S. flag

An official website of the United States government

nsv6734704

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,167

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 110 SVs from 20 studies. See in: genome view    
    Submitted genomic169,926,759-169,939,925Question Mark
    Overlapping variant regions from other studies: 110 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):169,644,547-169,657,713Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6734704Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3169,926,759169,939,925
    nsv6734704RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3169,644,547169,657,713

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18476487deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18476487Submitted genomicNC_000003.12:g.169
    926759_169939925de
    l
    GRCh38 (hg38)NC_000003.12Chr3169,926,759169,939,925
    nssv18476487RemappedPerfectNC_000003.11:g.169
    644547_169657713de
    l
    GRCh37.p13First PassNC_000003.11Chr3169,644,547169,657,713

    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)
    nssv184764874e-061276250
    Support Center