A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1142314



Internal ID18912087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:64096973..64097045hg38UCSC Ensembl
Outerchr20:62728326..62728398hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993815
SamplesKWS2
Known GenesOPRL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1142314
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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