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nsv6644034

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,293

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 136 SVs from 25 studies. See in: genome view    
    Submitted genomic169,559,405-169,560,697Question Mark
    Overlapping variant regions from other studies: 139 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):169,528,643-169,529,935Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6644034Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1169,559,405169,560,697
    nsv6644034RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1169,528,643169,529,935

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18583218duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18583218Submitted genomicNC_000001.11:g.169
    559405_169560697du
    p
    GRCh38 (hg38)NC_000001.11Chr1169,559,405169,560,697
    nssv18583218RemappedPerfectNC_000001.10:g.169
    528643_169529935du
    p
    GRCh37.p13First PassNC_000001.10Chr1169,528,643169,529,935

    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)
    nssv185832184e-061266800
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