A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3514912



Internal ID18813193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:30872741..30907727hg38UCSC Ensembl
Innerchr11:30894288..30929274hg19UCSC Ensembl
Innerchr11:30850864..30885850hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3834987
hg1934987
hg1834987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043222
Supporting Variants
Samples
Known GenesDCDC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3514912
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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