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nsv6897012

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,772

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 79 SVs from 22 studies. See in: genome view    
    Submitted genomic102,126,866-102,128,637Question Mark
    Overlapping variant regions from other studies: 79 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):103,886,623-103,888,394Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6897012Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10102,126,866102,128,637
    nsv6897012RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10103,886,623103,888,394

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18331164deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18331164Submitted genomicNC_000010.11:g.102
    126866_102128637de
    l
    GRCh38 (hg38)NC_000010.11Chr10102,126,866102,128,637
    nssv18331164RemappedPerfectNC_000010.10:g.103
    886623_103888394de
    l
    GRCh37.p13First PassNC_000010.10Chr10103,886,623103,888,394

    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)
    nssv183311644e-061272778
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