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nsv6897715

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:445

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 17 studies. See in: genome view    
    Submitted genomic119,371,956-119,372,400Question Mark
    Overlapping variant regions from other studies: 96 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):121,131,468-121,131,912Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6897715Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10119,371,956119,372,400
    nsv6897715RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10121,131,468121,131,912

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18583009duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18583009Submitted genomicNC_000010.11:g.119
    371956_119372400du
    p
    GRCh38 (hg38)NC_000010.11Chr10119,371,956119,372,400
    nssv18583009RemappedPerfectNC_000010.10:g.121
    131468_121131912du
    p
    GRCh37.p13First PassNC_000010.10Chr10121,131,468121,131,912

    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)
    nssv185830094e-061248700
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