A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963767



Internal ID19220768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:120061467..120061948hg38UCSC Ensembl
Outerchr11:119932176..119932657hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129527
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963767
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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