A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751636



Internal ID12985188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36103057..36145077hg38UCSC Ensembl
Innerchr17:34430450..34472462hg19UCSC Ensembl
Innerchr17:31454563..31496575hg18UCSC Ensembl
Innerchr17:31454563..31496575hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3842021
hg1942013
hg1842013
hg1742013
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv121e55
Supporting Variantsessv6985379, essv6987238
SamplesSPC_157
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)esv2751636
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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