A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35123



Internal ID12644473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31716782..32219354hg38UCSC Ensembl
Innerchr15:32008985..32511555hg19UCSC Ensembl
Innerchr15:29796277..30298847hg18UCSC Ensembl
Innerchr15:29796277..30298847hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38502573
hg19502571
hg18502571
hg17502571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv109e55
Supporting Variantsessv6978083, essv6986537, essv6978082, essv6990193
SamplesNA11830
Known GenesCHRNA7
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv35123
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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