A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3513369



Internal ID18811650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84732242..84796724hg38UCSC Ensembl
Innerchr11:84443285..84507767hg19UCSC Ensembl
Innerchr11:84120933..84185415hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3864483
hg1964483
hg1864483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041726
Supporting Variants
Samples
Known GenesDLG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3513369
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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