A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007202



Internal ID22068833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:79272928..79282708hg38UCSC Ensembl
Outerchr11:79270153..79290404hg38UCSC Ensembl
Innerchr11:78983973..78993753hg19UCSC Ensembl
Outerchr11:78981198..79001449hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3820252
hg1920252
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154748
Supporting Variants
Samples
Known GenesTENM4
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007202
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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