A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155966



Internal ID22086471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:57973098..57992224hg38UCSC Ensembl
Outerchr3:57964916..57992526hg38UCSC Ensembl
Innerchr3:57958825..57977951hg19UCSC Ensembl
Outerchr3:57950643..57978253hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3827611
hg1927611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016385
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155966
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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