A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv180n97



Internal ID22815577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47143452..47161314hg38UCSC Ensembl
chr20:45772091..45789953hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3817863
hg1917863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155653, nsv1155654
Samples
Known GenesEYA2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv180n97
Frequency
Sample Size131
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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