A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697509



Internal ID121175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84500197..84505699hg38UCSC Ensembl
chr14:84966541..84972043hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg385503
hg195503
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697509
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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