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nsv6606168

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:360,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1147 SVs from 76 studies. See in: genome view    
    Submitted genomic101,725,501-102,085,900Question Mark
    Overlapping variant regions from other studies: 1147 SVs from 76 studies. See in: genome view    
    Remapped(Score: Perfect):102,173,376-102,533,775Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6606168Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6101,725,501102,085,900
    nsv6606168RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6102,173,376102,533,775

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18136708deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18136708Submitted genomicNC_000006.12:g.101
    725501_102085900de
    l
    GRCh38 (hg38)NC_000006.12Chr6101,725,501102,085,900
    nssv18136708RemappedPerfectNC_000006.11:g.102
    173376_102533775de
    l
    GRCh37.p13First PassNC_000006.11Chr6102,173,376102,533,775

    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)
    nssv18136708<0.001139106
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