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nsv6351038

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:621,588

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2222 SVs from 83 studies. See in: genome view    
    Submitted genomic169,420,756-170,042,343Question Mark
    Overlapping variant regions from other studies: 2222 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):170,277,266-170,898,853Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6351038Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2169,420,756170,042,343
    nsv6351038RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2170,277,266170,898,853

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18079971deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18079971Submitted genomicNC_000002.12:g.169
    420756_170042343de
    l
    GRCh38 (hg38)NC_000002.12Chr2169,420,756170,042,343
    nssv18079971RemappedPerfectNC_000002.11:g.170
    277266_170898853de
    l
    GRCh37.p13First PassNC_000002.11Chr2170,277,266170,898,853

    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)
    nssv18079971<0.001139152
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