A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4285n100



Internal ID22790372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22061780..22174297hg38UCSC Ensembl
chr20:22042418..22154935hg19UCSC Ensembl
chr20:21990418..22102935hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38112518
hg19112518
hg18112518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056616, nsv1058614, nsv1057093, nsv1064957, nsv1058372
Samples
Known GenesLOC100270679
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4285n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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