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nsv6676890

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:79,866

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 292 SVs from 38 studies. See in: genome view    
    Submitted genomic23,963,439-24,043,304Question Mark
    Overlapping variant regions from other studies: 292 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):24,186,309-24,266,174Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6676890Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr223,963,43924,043,304
    nsv6676890RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr224,186,30924,266,174

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18463055deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18463055Submitted genomicNC_000002.12:g.239
    63439_24043304del
    GRCh38 (hg38)NC_000002.12Chr223,963,43924,043,304
    nssv18463055RemappedPerfectNC_000002.11:g.241
    86309_24266174del
    GRCh37.p13First PassNC_000002.11Chr224,186,30924,266,174

    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)
    nssv184630554e-061276248
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