A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518424



Internal ID15099031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:23422570..23507347hg38UCSC Ensembl
InnerchrX:23440687..23525464hg19UCSC Ensembl
InnerchrX:23350608..23435385hg18UCSC Ensembl
InnerchrX:23200344..23285121hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3884778
hg1984778
hg1884778
hg1784778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695859
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518424
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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