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nsv6890945

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:49

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 19 studies. See in: genome view    
    Submitted genomic17,871,708-17,871,756Question Mark
    Overlapping variant regions from other studies: 3 SVs from 3 studies. See in: genome view    
    Remapped(Score: Perfect):300,499-300,547Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6890945Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1017,871,70817,871,756
    nsv6890945RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315932.1Chr10|NW_0
    03315932.1
    300,499300,547

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18334064deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18334064Submitted genomicNC_000010.11:g.178
    71708_17871756del
    GRCh38 (hg38)NC_000010.11Chr1017,871,70817,871,756
    nssv18334064RemappedPerfectNW_003315932.1:g.3
    00499_300547del
    GRCh37.p13First PassNW_003315932.1Chr10|NW_0
    03315932.1
    300,499300,547

    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)
    nssv183340644e-061254214
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