A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17728767



Internal ID152433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36357097..36357178hg38UCSC Ensembl
chr22:36753142..36753223hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553464
Supporting Variants
Samples
Known GenesMYH9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17728767
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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