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nsv6355457

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 201 SVs from 37 studies. See in: genome view    
    Submitted genomic169,503,801-169,509,300Question Mark
    Overlapping variant regions from other studies: 201 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):170,360,311-170,365,810Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6355457Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2169,503,801169,509,300
    nsv6355457RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2170,360,311170,365,810

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18207384duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18207384Submitted genomicNC_000002.12:g.169
    503801_169509300du
    p
    GRCh38 (hg38)NC_000002.12Chr2169,503,801169,509,300
    nssv18207384RemappedPerfectNC_000002.11:g.170
    360311_170365810du
    p
    GRCh37.p13First PassNC_000002.11Chr2170,360,311170,365,810

    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)
    nssv18207384<0.001339188
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