A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983716



Internal ID18896678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125025001..125025073hg38UCSC Ensembl
Outerchr11:124894897..124894969hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125537
Supporting Variants
SamplesKWS2
Known GenesCCDC15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983716
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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