A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152692



Internal ID18854861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:89859331..89887032hg38UCSC Ensembl
Outerchr11:89592499..89620200hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3827702
hg1927702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999874
SamplesKWB1
Known GenesMIR5692A1, TRIM64B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152692
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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