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nsv6934528

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,606

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 24 studies. See in: genome view    
    Submitted genomic106,792,647-106,794,252Question Mark
    Overlapping variant regions from other studies: 82 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):107,186,425-107,188,030Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6934528Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12106,792,647106,794,252
    nsv6934528RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12107,186,425107,188,030

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18356162deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18356162Submitted genomicNC_000012.12:g.106
    792647_106794252de
    l
    GRCh38 (hg38)NC_000012.12Chr12106,792,647106,794,252
    nssv18356162RemappedPerfectNC_000012.11:g.107
    186425_107188030de
    l
    GRCh37.p13First PassNC_000012.11Chr12107,186,425107,188,030

    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)
    nssv183561624e-061272938
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