A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3322n100



Internal ID22789409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14071214..14233523hg38UCSC Ensembl
chr18:14071213..14233522hg19UCSC Ensembl
chr18:14061213..14223522hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38162310
hg19162310
hg18162310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063794, nsv1058322, nsv1063978
Samples
Known GenesANKRD20A5P, ZNF519
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3322n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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