A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956233



Internal ID22731425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39707155..39710197hg38UCSC Ensembl
chr22:40103160..40106202hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383043
hg193043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390127
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956233
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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