A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17697394



Internal ID121060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102092348..102093022hg38UCSC Ensembl
chr14:102558685..102559359hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512409
Supporting Variants
Samples
Known GenesHSP90AA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17697394
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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