A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710673



Internal ID19008954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:84381684..84563646hg38UCSC Ensembl
Innerchr11:84092727..84274689hg19UCSC Ensembl
Innerchr11:83770375..83952337hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38181963
hg19181963
hg18181963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052925
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)nssv3710673
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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