A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696795



Internal ID120461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34077626..34088561hg38UCSC Ensembl
chr14:34546832..34557767hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3810936
hg1910936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504244
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696795
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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