A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452837



Internal ID230980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14480215..14500205hg38UCSC Ensembl
chr2:14620339..14640329hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3819991
hg1919991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452837
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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