A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957759



Internal ID22732870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36468682..36468998hg38UCSC Ensembl
chr22:36864729..36865045hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409474
Samples
Known GenesTXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957759
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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