A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143665



Internal ID18910397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:416400..417400hg38UCSC Ensembl
Outerchr11:416400..417400hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994352
SamplesKWS1
Known GenesSIGIRR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143665
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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