A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443519



Internal ID221915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36119000..36343619hg38UCSC Ensembl
chr2:36346143..36570762hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38224620
hg19224620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16912130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443519
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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