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nsv6962408

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:23,450

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 24 studies. See in: genome view    
    Submitted genomic48,927,581-48,951,030Question Mark
    Overlapping variant regions from other studies: 137 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):49,219,778-49,243,227Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6962408Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1548,927,58148,951,030
    nsv6962408RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1549,219,77849,243,227

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18394029deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18394029Submitted genomicNC_000015.10:g.489
    27581_48951030del
    GRCh38 (hg38)NC_000015.10Chr1548,927,58148,951,030
    nssv18394029RemappedPerfectNC_000015.9:g.4921
    9778_49243227del
    GRCh37.p13First PassNC_000015.9Chr1549,219,77849,243,227

    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)
    nssv183940294e-061275976
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