A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450655



Internal ID228857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:205949901..205950514hg38UCSC Ensembl
chr2:206814625..206815238hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38614
hg19614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16922957
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450655
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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