A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980921



Internal ID12635590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22808784..23500295hg38UCSC Ensembl
Innerchr19:22991586..23683097hg19UCSC Ensembl
Innerchr19:22783426..23474937hg18UCSC Ensembl
Innerchr19:22783426..23474937hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38691512
hg19691512
hg18691512
hg17691512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34907
Supporting Variants
SamplesNA19144
Known GenesLOC100132815, ZNF724P, ZNF728, ZNF730, ZNF91
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980921
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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