A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695886



Internal ID119552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58578336..58589942hg38UCSC Ensembl
chr14:59045054..59056660hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3811607
hg1911607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505325
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695886
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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