A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979241



Internal ID18881802
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 StatusS
Merged Variantsnsv1116676
Supporting Variants
SamplesKWS2
Known GenesCD5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979241
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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