A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910495



Internal ID7769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21181280..21193375hg38UCSC Ensembl
chr2:21404152..21416247hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3812096
hg1912096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910495
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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