A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926028



Internal ID18096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219931809..219937618hg38UCSC Ensembl
chr2:220796530..220802339hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg385810
hg195810
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139901
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926028
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.075325


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