A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16919724



Internal ID13937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:114101733..114101793hg38UCSC Ensembl
chr2:114859310..114859370hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440738
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16919724
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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