A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011886



Internal ID22073517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22523791..22528537hg38UCSC Ensembl
Outerchr18:22521703..22535891hg38UCSC Ensembl
Innerchr18:20103754..20108500hg19UCSC Ensembl
Outerchr18:20101666..20115854hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3814189
hg1914189
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155504
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011886
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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