A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145571



Internal ID18910787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:118910894..118910946hg38UCSC Ensembl
Outerchr11:118781603..118781655hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv732n106
Supporting Variantsnssv3983219
SamplesKWS1
Known GenesBCL9L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145571
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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