A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3979251



Internal ID18885321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:132125729..132125791hg38UCSC Ensembl
Outerchr11:131995623..131995685hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116687
Supporting Variants
SamplesKWS2
Known GenesNTM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3979251
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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