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nsv6903444

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,499,617

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5491 SVs from 116 studies. See in: genome view    
    Submitted genomic24,768,508-26,268,124Question Mark
    Overlapping variant regions from other studies: 5493 SVs from 116 studies. See in: genome view    
    Remapped(Score: Perfect):24,790,054-26,289,671Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6903444Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1124,768,50826,268,124
    nsv6903444RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1124,790,05426,289,671

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18348154deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18348154Submitted genomicNC_000011.10:g.247
    68508_26268124del
    GRCh38 (hg38)NC_000011.10Chr1124,768,50826,268,124
    nssv18348154RemappedPerfectNC_000011.9:g.2479
    0054_26289671del
    GRCh37.p13First PassNC_000011.9Chr1124,790,05426,289,671

    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)
    nssv183481544e-061272942
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