A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1140464



Internal ID18924253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:696675..696796hg38UCSC Ensembl
Outerchr11:696675..696796hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3979172
SamplesKWS2
Known GenesTMEM80
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1140464
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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