A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148110



Internal ID18854075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:176599..196800hg38UCSC Ensembl
Outerchr11:176599..196800hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3820202
hg1920202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001622
SamplesKWB1
Known GenesLOC653486, ODF3, SCGB1C1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148110
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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