A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16928537



Internal ID19740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:230977931..230978064hg38UCSC Ensembl
chr2:231842646..231842779hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438032
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16928537
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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