A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5550869



Internal ID324370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37508887..37508950hg38UCSC Ensembl
chr22:37904894..37904957hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17728839
Samples
Known GenesCARD10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5550869
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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