A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001622



Internal ID18845654
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 StatusS
Merged Variantsnsv1148110
Supporting Variants
SamplesKWB1
Known GenesLOC653486, ODF3, SCGB1C1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001622
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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