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nsv6727962

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:235,912

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 837 SVs from 67 studies. See in: genome view    
    Submitted genomic194,215,451-194,451,362Question Mark
    Overlapping variant regions from other studies: 814 SVs from 67 studies. See in: genome view    
    Remapped(Score: Good):193,933,240-194,172,091Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6727962Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3194,215,451194,451,362
    nsv6727962RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3193,933,240194,172,091

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18676637duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18676637Submitted genomicNC_000003.12:g.194
    215451_194451362du
    p
    GRCh38 (hg38)NC_000003.12Chr3194,215,451194,451,362
    nssv18676637RemappedGoodNC_000003.11:g.193
    933240_194172091du
    p
    GRCh37.p13First PassNC_000003.11Chr3193,933,240194,172,091

    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)
    nssv186766374e-061275912
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