A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922058



Internal ID15469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191956905..191956974hg38UCSC Ensembl
chr2:192821631..192821700hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445810
Supporting Variants
Samples
Known GenesTMEFF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922058
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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