A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134159



Internal ID18931992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:83507417..83507471hg38UCSC Ensembl
Outerchr11:83218460..83218514hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv681n106
Supporting Variantsnssv3970503
SamplesKWS2
Known GenesDLG2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134159
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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