A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7153n100



Internal ID20158769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27780880..27831551hg38UCSC Ensembl
chr8:27638397..27689068hg19UCSC Ensembl
chr8:27694316..27744987hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3850672
hg1950672
hg1850672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026852, nsv1023045, nsv1022209
Samples
Known GenesESCO2, PBK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7153n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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