A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005018



Internal ID17297970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:58453115..58453440hg38UCSC Ensembl
Outerchr11:58220588..58220913hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957204
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005018
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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