A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988826



Internal ID21898169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26558786..26563266hg38UCSC Ensembl
chr2:26781654..26786134hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg384481
hg194481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535758
Samples
Known GenesC2orf70
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988826
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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