A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751785



Internal ID12985337
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 StatusM
Merged Variants
Supporting Variantsessv6989396, essv6989871, essv6983873
SamplesBEC_727
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751785
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer