A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986688



Internal ID12632262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3838380..4072950hg38UCSC Ensembl
Innerchr18:3838380..4072950hg19UCSC Ensembl
Innerchr18:3828380..4062950hg18UCSC Ensembl
Innerchr18:3828380..4062950hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38234571
hg19234571
hg18234571
hg17234571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34571
Supporting Variants
SamplesNA12145
Known GenesDLGAP1, DLGAP1-AS3, DLGAP1-AS4, MIR6718
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986688
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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