A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698389



Internal ID122055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102731370..102737797hg38UCSC Ensembl
chr14:103197707..103204134hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg386428
hg196428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511971
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698389
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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