A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5449609



Internal ID227842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6303918..6304137hg38UCSC Ensembl
chr2:6444050..6444269hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5449609
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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