A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923693



Internal ID16559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201292036..201301432hg38UCSC Ensembl
chr2:202156759..202166155hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg389397
hg199397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437794
Supporting Variants
Samples
Known GenesALS2CR12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923693
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003904


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