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nsv7076914

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,770

    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 genomic28,733,178-28,737,947Question Mark
    Overlapping variant regions from other studies: 102 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):27,060,196-27,064,965Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7076914Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1728,733,17828,737,947
    nsv7076914RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1727,060,19627,064,965

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756927inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756927Submitted genomicNC_000017.11:g.287
    33178_28737947inv
    GRCh38 (hg38)NC_000017.11Chr1728,733,17828,737,947
    nssv18756927RemappedPerfectNC_000017.10:g.270
    60196_27064965inv
    GRCh37.p13First PassNC_000017.10Chr1727,060,19627,064,965

    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)
    nssv187569274e-061276268
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