A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153572



Internal ID19202040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:60602626..60604727hg38UCSC Ensembl
Outerchr11:60370099..60372200hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382102
hg192102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002226
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153572
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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