A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962588



Internal ID19216318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:120328595..120328681hg38UCSC Ensembl
Outerchr11:120199304..120199390hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129158
Supporting Variants
SamplesKWS1
Known GenesTMEM136
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962588
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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