A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999874



Internal ID18843795
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 StatusS
Merged Variantsnsv1152692
Supporting Variants
SamplesKWB1
Known GenesMIR5692A1, TRIM64B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999874
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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