A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001695



Internal ID19190177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:39126349..39131850hg38UCSC Ensembl
Outerchr11:39147899..39153400hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385502
hg195502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148186
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001695
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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