A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151044



Internal ID19198182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:54525380..54547381hg38UCSC Ensembl
Outerchr11:51571899..51593900hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3822002
hg1922002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001977
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151044
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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