A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005566



Internal ID22067197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4228783..4338058hg38UCSC Ensembl
Outerchr11:4217824..4363567hg38UCSC Ensembl
Innerchr11:4250013..4359288hg19UCSC Ensembl
Outerchr11:4239054..4384797hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38145744
hg19145744
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154673
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005566
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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