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nsv6892477

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 66 SVs from 13 studies. See in: genome view    
    Submitted genomic102,129,972-102,130,035Question Mark
    Overlapping variant regions from other studies: 66 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):103,889,729-103,889,792Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6892477Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10102,129,972102,130,035
    nsv6892477RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10103,889,729103,889,792

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18331165deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18331165Submitted genomicNC_000010.11:g.102
    129972_102130035de
    l
    GRCh38 (hg38)NC_000010.11Chr10102,129,972102,130,035
    nssv18331165RemappedPerfectNC_000010.10:g.103
    889729_103889792de
    l
    GRCh37.p13First PassNC_000010.10Chr10103,889,729103,889,792

    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)
    nssv183311657e-062267908
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