A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv111e55



Internal ID22761061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87219818..87335372hg38UCSC Ensembl
chr15:87763049..87878603hg19UCSC Ensembl
chr15:85564053..85679607hg18UCSC Ensembl
chr15:85564053..85679607hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38115555
hg19115555
hg18115555
hg17115555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2751540, esv2751539
SamplesSPC_179, BEC_400
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv111e55
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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