A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv161e55



Internal ID22761111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141423699..141481699hg38UCSC Ensembl
chr2:142181268..142239268hg19UCSC Ensembl
chr2:141897738..141955738hg18UCSC Ensembl
chr2:142015000..142073000hg17UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3858001
hg1958001
hg1858001
hg1758001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34606, esv34823
SamplesNA18501, NA18500
Known GenesLRP1B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv161e55
Frequency
Sample Size771
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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