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nsv6349211

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:629,993

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1575 SVs from 75 studies. See in: genome view    
    Submitted genomic102,073,096-102,703,088Question Mark
    Overlapping variant regions from other studies: 1575 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):102,689,556-103,319,547Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6349211Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2102,073,096102,703,088
    nsv6349211RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2102,689,556103,319,547

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18205777duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18205777Submitted genomicNC_000002.12:g.102
    073096_102703088du
    p
    GRCh38 (hg38)NC_000002.12Chr2102,073,096102,703,088
    nssv18205777RemappedPerfectNC_000002.11:g.102
    689556_103319547du
    p
    GRCh37.p13First PassNC_000002.11Chr2102,689,556103,319,547

    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)
    nssv18205777<0.001239302
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