A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16921601



Internal ID15168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157445477..157454156hg38UCSC Ensembl
chr2:158301989..158310668hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg388680
hg198680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16921601
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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