A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155653



Internal ID22086158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47144639..47160290hg38UCSC Ensembl
Outerchr20:47143452..47161314hg38UCSC Ensembl
Innerchr20:45773278..45788929hg19UCSC Ensembl
Outerchr20:45772091..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 Variantsdgv180n97
Supporting Variantsnssv4013885
Samples
Known GenesEYA2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155653
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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