A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985779



Internal ID12984032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36103057..36150004hg38UCSC Ensembl
Innerchr17:34430450..34477386hg19UCSC Ensembl
Innerchr17:31454563..31501499hg18UCSC Ensembl
Innerchr17:31454563..31501499hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3846948
hg1946937
hg1846937
hg1746937
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35032
Supporting Variants
SamplesSPC_47
Known GenesCCL4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985779
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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