A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999066



Internal ID19194930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63420127..63435428hg38UCSC Ensembl
Outerchr11:63187599..63202900hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3815302
hg1915302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151883
Supporting Variants
SamplesKWB1
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999066
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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