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nsv6440568

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,789

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 80 SVs from 16 studies. See in: genome view    
    Submitted genomic102,154,928-102,157,716Question Mark
    Overlapping variant regions from other studies: 80 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):103,914,685-103,917,473Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6440568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10102,154,928102,157,716
    nsv6440568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10103,914,685103,917,473

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17977244deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17977244Submitted genomicNC_000010.11:g.102
    154928_102157716de
    l
    GRCh38 (hg38)NC_000010.11Chr10102,154,928102,157,716
    nssv17977244RemappedPerfectNC_000010.10:g.103
    914685_103917473de
    l
    GRCh37.p13First PassNC_000010.10Chr10103,914,685103,917,473

    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)
    nssv17977244<0.001138864
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