A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3321n100



Internal ID22789408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14062273..14304890hg38UCSC Ensembl
chr18:14062272..14304889hg19UCSC Ensembl
chr18:14052272..14294889hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38242618
hg19242618
hg18242618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066363, nsv1063019, nsv1060497, nsv1064422, nsv1055996, nsv1055190
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)dgv3321n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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