A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34941



Internal ID12990977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36103020..36150004hg38UCSC Ensembl
Innerchr17:34430413..34477386hg19UCSC Ensembl
Innerchr17:31454526..31501499hg18UCSC Ensembl
Innerchr17:31454526..31501499hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3846985
hg1946974
hg1846974
hg1746974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv121e55
Supporting Variantsessv6980115, essv6987006, essv6980114
SamplesNA18956
Known GenesCCL4
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)esv34941
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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