A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923882



Internal ID16685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218174323..218179846hg38UCSC Ensembl
chr2:219039046..219044569hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg385524
hg195524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449026
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923882
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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