A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984935



Internal ID12637062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51782535..52069835hg38UCSC Ensembl
Innerchr19:52285788..52573088hg19UCSC Ensembl
Innerchr19:56977600..57264900hg18UCSC Ensembl
Innerchr19:56977600..57264900hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38287301
hg19287301
hg18287301
hg17287301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751801
Supporting Variants
SamplesSPC_195
Known GenesFPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF649, ZNF841
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984935
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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