A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985538



Internal ID21894881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109033970..109070589hg38UCSC Ensembl
chr2:109650426..109687045hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3836620
hg1936620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985538
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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