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nsv6478848

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:375

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 153 SVs from 12 studies. See in: genome view    
    Submitted genomic102,371,839-102,372,213Question Mark
    Overlapping variant regions from other studies: 153 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):103,024,189-103,024,563Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6478848Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr13102,371,839102,372,213
    nsv6478848RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr13103,024,189103,024,563

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18006372deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18006372Submitted genomicNC_000013.11:g.102
    371839_102372213de
    l
    GRCh38 (hg38)NC_000013.11Chr13102,371,839102,372,213
    nssv18006372RemappedPerfectNC_000013.10:g.103
    024189_103024563de
    l
    GRCh37.p13First PassNC_000013.10Chr13103,024,189103,024,563

    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)
    nssv18006372<0.0012737848
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