A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981292



Internal ID12626444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36044950..36150005hg38UCSC Ensembl
Innerchr17:34371987..34477387hg19UCSC Ensembl
Innerchr17:31396100..31501500hg18UCSC Ensembl
Innerchr17:31396100..31501500hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38105056
hg19105401
hg18105401
hg17105401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751623
Supporting Variants
SamplesBEC_379
Known GenesCCL18, CCL3, CCL4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981292
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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