A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115053



Internal ID21298319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:41126151..41131646hg38UCSC Ensembl
Innerchr2:41353291..41358786hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg385496
hg195496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102525
Samplessample63
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115053
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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