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nsv7013548

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,903

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 47 studies. See in: genome view    
    Submitted genomic51,463,369-51,511,271Question Mark
    Overlapping variant regions from other studies: 193 SVs from 47 studies. See in: genome view    
    Remapped(Score: Perfect):51,966,623-52,014,525Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7013548Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1951,463,36951,511,271
    nsv7013548RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1951,966,62352,014,525

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638748duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638748Submitted genomicNC_000019.10:g.514
    63369_51511271dup
    GRCh38 (hg38)NC_000019.10Chr1951,463,36951,511,271
    nssv18638748RemappedPerfectNC_000019.9:g.5196
    6623_52014525dup
    GRCh37.p13First PassNC_000019.9Chr1951,966,62352,014,525

    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)
    nssv186387487e-062275908
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