A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511804



Internal ID18463399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113387343..113415194hg38UCSC Ensembl
Innerchr11:113258065..113285916hg19UCSC Ensembl
Innerchr11:112763275..112791126hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3827852
hg1927852
hg1827852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040152
Supporting Variants
Samples
Known GenesANKK1, DRD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511804
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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