A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985965



Internal ID12637613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51782576..52101372hg38UCSC Ensembl
Innerchr19:52285829..52604625hg19UCSC Ensembl
Innerchr19:56977641..57296437hg18UCSC Ensembl
Innerchr19:56977641..57296437hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38318797
hg19318797
hg18318797
hg17318797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751799
Supporting Variants
SamplesSPC_88
Known GenesFPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF649, ZNF841
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985965
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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