A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118215



Internal ID18918997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67266429..67266829hg38UCSC Ensembl
Outerchr11:67033900..67034300hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980884
SamplesKWS1
Known GenesADRBK1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118215
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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