A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518944



Internal ID15446237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:27831821..28014899hg38UCSC Ensembl
InnerchrX:27849938..28033016hg19UCSC Ensembl
InnerchrX:27759859..27942937hg18UCSC Ensembl
InnerchrX:27609595..27792673hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38183079
hg19183079
hg18183079
hg17183079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696411
Samples
Known GenesDCAF8L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518944
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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