A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452686



Internal ID230832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85406274..85406383hg38UCSC Ensembl
chr2:85633397..85633506hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16917346
Samples
Known GenesCAPG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452686
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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