A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5438205



Internal ID216774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15002590..15002640hg38UCSC Ensembl
chr2:15142714..15142764hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16910103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5438205
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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