A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960538



Internal ID22735511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42367239..42372457hg38UCSC Ensembl
chr22:42763245..42768463hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg385219
hg195219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960538
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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