A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698800



Internal ID122466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100466717..100467980hg38UCSC Ensembl
chr14:100933054..100934317hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511369
Supporting Variants
Samples
Known GenesWDR25
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698800
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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