A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696817



Internal ID120483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34369265..34374664hg38UCSC Ensembl
chr14:34838471..34843870hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503666
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696817
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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