A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695523



Internal ID119189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34903287..34906305hg38UCSC Ensembl
chr14:35372493..35375511hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg383019
hg193019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695523
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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