A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695873



Internal ID119539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58269196..58269430hg38UCSC Ensembl
chr14:58735914..58736148hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502482
Supporting Variants
Samples
Known GenesFLJ31306, PSMA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695873
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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