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nsv6790359

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:653

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 112 SVs from 23 studies. See in: genome view    
    Submitted genomic126,565,857-126,566,509Question Mark
    Overlapping variant regions from other studies: 112 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):125,901,549-125,902,201Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6790359Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5126,565,857126,566,509
    nsv6790359RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5125,901,549125,902,201

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18694684duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18694684Submitted genomicNC_000005.10:g.126
    565857_126566509du
    p
    GRCh38 (hg38)NC_000005.10Chr5126,565,857126,566,509
    nssv18694684RemappedPerfectNC_000005.9:g.1259
    01549_125902201dup
    GRCh37.p13First PassNC_000005.9Chr5125,901,549125,902,201

    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)
    nssv186946841.2e-053246262
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