A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116676



Internal ID18940192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:61104050..61104130hg38UCSC Ensembl
Outerchr11:60871522..60871602hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979241
SamplesKWS2
Known GenesCD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116676
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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