A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517473



Internal ID18815754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120353835..120405664hg38UCSC Ensembl
Innerchr11:120224544..120276373hg19UCSC Ensembl
Innerchr11:119729754..119781583hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3851830
hg1951830
hg1851830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050935
Supporting Variants
Samples
Known GenesARHGEF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3517473
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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