A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915694



Internal ID11195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:83883829..83883951hg38UCSC Ensembl
chr2:84110953..84111075hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915694
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.039206


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