A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4287n100



Internal ID22790374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23734421..23816014hg38UCSC Ensembl
chr20:23715058..23796651hg19UCSC Ensembl
chr20:23663058..23744651hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3881594
hg1981594
hg1881594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063895, nsv1065355
Samples
Known GenesCST1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4287n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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