A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693945



Internal ID117611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22965481..22966342hg38UCSC Ensembl
chr14:23434690..23435551hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497105
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693945
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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