A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155663



Internal ID22086168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64323342..64324800hg38UCSC Ensembl
Outerchr20:64284715..64324800hg38UCSC Ensembl
Innerchr20:62954695..62956153hg19UCSC Ensembl
Outerchr20:62916068..62956153hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3840086
hg1940086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013916, nssv4013917
Samples
Known GenesLINC00266-1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155663
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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