A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922895



Internal ID16023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202234810..202234881hg38UCSC Ensembl
chr2:203099533..203099604hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442623
Supporting Variants
Samples
Known GenesSUMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922895
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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