A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156058



Internal ID22086563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:185383634..185392420hg38UCSC Ensembl
Outerchr3:185381642..185394512hg38UCSC Ensembl
Innerchr3:185101422..185110208hg19UCSC Ensembl
Outerchr3:185099430..185112300hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3812871
hg1912871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017222
Samples
Known GenesMAP3K13
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156058
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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