A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959456



Internal ID19207774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:131500..135500hg38UCSC Ensembl
Outerchr11:131500..135500hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384001
hg194001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110189
Supporting Variants
SamplesKWS1
Known GenesLINC01001
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959456
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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