A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110190



Internal ID18908829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:160800..196800hg38UCSC Ensembl
Outerchr11:160800..196800hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3836001
hg1936001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959457
SamplesKWS1
Known GenesLOC653486, ODF3, SCGB1C1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110190
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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