A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007230



Internal ID22068861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86176915..86188770hg38UCSC Ensembl
Outerchr11:86174680..86191421hg38UCSC Ensembl
Innerchr11:85887957..85899812hg19UCSC Ensembl
Outerchr11:85885722..85902463hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3816742
hg1916742
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154753
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007230
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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