A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990195



Internal ID12631938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51782576..52127682hg38UCSC Ensembl
Innerchr19:52285829..52630935hg19UCSC Ensembl
Innerchr19:56977641..57322747hg18UCSC Ensembl
Innerchr19:56977641..57322747hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38345107
hg19345107
hg18345107
hg17345107
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34938
Supporting Variants
SamplesNA11832
Known GenesFPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF616, ZNF649, ZNF841
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990195
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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