A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965202



Internal ID22740137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30914328..30917036hg38UCSC Ensembl
chr22:31310315..31313023hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg382709
hg192709
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965202
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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