A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986264



Internal ID21895607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149477299..149478183hg38UCSC Ensembl
chr2:150333813..150334697hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986264
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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