A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695766



Internal ID119432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:26984229..27061139hg38UCSC Ensembl
chr14:27453435..27530345hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3876911
hg1976911
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512997
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695766
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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