A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv259e55



Internal ID22761209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28166402..28380169hg38UCSC Ensembl
chr9:28166400..28380167hg19UCSC Ensembl
chr9:28156400..28370167hg18UCSC Ensembl
chr9:28156400..28370167hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38213768
hg19213768
hg18213768
hg17213768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2752292, esv2752293, esv2752294
SamplesBEC_704, BEC_451, BEC_628
Known GenesLINGO2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv259e55
Frequency
Sample Size771
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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