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nsv6325898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 25 studies. See in: genome view    
    Submitted genomic19,611,801-19,612,600Question Mark
    Overlapping variant regions from other studies: 106 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):19,938,295-19,939,094Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6325898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,611,80119,612,600
    nsv6325898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr119,938,29519,939,094

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18056458deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18056458Submitted genomicNC_000001.11:g.196
    11801_19612600del
    GRCh38 (hg38)NC_000001.11Chr119,611,80119,612,600
    nssv18056458RemappedPerfectNC_000001.10:g.199
    38295_19939094del
    GRCh37.p13First PassNC_000001.10Chr119,938,29519,939,094

    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)
    nssv18056458<0.001127300
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