A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982157



Internal ID12626614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36045750..36145102hg38UCSC Ensembl
Innerchr17:34372787..34472487hg19UCSC Ensembl
Innerchr17:31396900..31496600hg18UCSC Ensembl
Innerchr17:31396900..31496600hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3899353
hg1999701
hg1899701
hg1799701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751624
Supporting Variants
SamplesBEC_397
Known GenesCCL18, CCL3, CCL4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982157
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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