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nsv6328210

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,095

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 27 studies. See in: genome view    
    Submitted genomic37,628,829-37,631,923Question Mark
    Overlapping variant regions from other studies: 111 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):38,094,501-38,097,595Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6328210Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr137,628,82937,631,923
    nsv6328210RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr138,094,50138,097,595

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18061203deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18061203Submitted genomicNC_000001.11:g.376
    28829_37631923del
    GRCh38 (hg38)NC_000001.11Chr137,628,82937,631,923
    nssv18061203RemappedPerfectNC_000001.10:g.380
    94501_38097595del
    GRCh37.p13First PassNC_000001.10Chr138,094,50138,097,595

    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)
    nssv18061203<0.001139058
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