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nsv6530389

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,014

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 26 studies. See in: genome view    
    Submitted genomic18,255,492-18,258,505Question Mark
    Overlapping variant regions from other studies: 120 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):18,366,302-18,369,315Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6530389Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1918,255,49218,258,505
    nsv6530389RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1918,366,30218,369,315

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18045079deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18045079Submitted genomicNC_000019.10:g.182
    55492_18258505del
    GRCh38 (hg38)NC_000019.10Chr1918,255,49218,258,505
    nssv18045079RemappedPerfectNC_000019.9:g.1836
    6302_18369315del
    GRCh37.p13First PassNC_000019.9Chr1918,366,30218,369,315

    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)
    nssv18045079<0.001139076
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