A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990036



Internal ID21899379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77001421..77006450hg38UCSC Ensembl
chr2:77228547..77233576hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg385030
hg195030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520637
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990036
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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