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nsv6642230

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,392

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 119 SVs from 27 studies. See in: genome view    
    Submitted genomic153,562,640-153,565,031Question Mark
    Overlapping variant regions from other studies: 130 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):153,535,116-153,537,507Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6642230Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1153,562,640153,565,031
    nsv6642230RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1153,535,116153,537,507

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18363538deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18363538Submitted genomicNC_000001.11:g.153
    562640_153565031de
    l
    GRCh38 (hg38)NC_000001.11Chr1153,562,640153,565,031
    nssv18363538RemappedPerfectNC_000001.10:g.153
    535116_153537507de
    l
    GRCh37.p13First PassNC_000001.10Chr1153,535,116153,537,507

    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)
    nssv183635384e-061272712
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