A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17695079



Internal ID118745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42417101..42417158hg38UCSC Ensembl
chr14:42886304..42886361hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501918
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17695079
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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