A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151296



Internal ID19201109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5738879..5741138hg38UCSC Ensembl
Outerchr11:5760109..5762368hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382260
hg192260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003855
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151296
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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