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nsv6895309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:44,390

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 161 SVs from 30 studies. See in: genome view    
    Submitted genomic102,480,383-102,524,772Question Mark
    Overlapping variant regions from other studies: 161 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):104,240,140-104,284,529Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6895309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10102,480,383102,524,772
    nsv6895309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10104,240,140104,284,529

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18581500duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18581500Submitted genomicNC_000010.11:g.102
    480383_102524772du
    p
    GRCh38 (hg38)NC_000010.11Chr10102,480,383102,524,772
    nssv18581500RemappedPerfectNC_000010.10:g.104
    240140_104284529du
    p
    GRCh37.p13First PassNC_000010.10Chr10104,240,140104,284,529

    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)
    nssv185815004e-061276000
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