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nsv6643122

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 102 SVs from 19 studies. See in: genome view    
    Submitted genomic160,260,563-160,260,589Question Mark
    Overlapping variant regions from other studies: 106 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):160,230,353-160,230,379Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643122Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,260,563160,260,589
    nsv6643122RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,230,353160,230,379

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18362648deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18362648Submitted genomicNC_000001.11:g.160
    260563_160260589de
    l
    GRCh38 (hg38)NC_000001.11Chr1160,260,563160,260,589
    nssv18362648RemappedPerfectNC_000001.10:g.160
    230353_160230379de
    l
    GRCh37.p13First PassNC_000001.10Chr1160,230,353160,230,379

    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)
    nssv183626480.0081712228154
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