A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987439



Internal ID21896782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211348471..211348559hg38UCSC Ensembl
chr2:212213196..212213284hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987439
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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