A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927558



Internal ID19086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187315845..187316220hg38UCSC Ensembl
chr2:188180572..188180947hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450486
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927558
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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