A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983873



Internal ID12977323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28184432..28278712hg38UCSC Ensembl
Innerchr19:28675339..28769619hg19UCSC Ensembl
Innerchr19:33367179..33461459hg18UCSC Ensembl
Innerchr19:33367179..33461459hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3894281
hg1994281
hg1894281
hg1794281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751785
Supporting Variants
SamplesBEC_727
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983873
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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