A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17693989



Internal ID117655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23728690..23739590hg38UCSC Ensembl
chr14:24197899..24208799hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3810901
hg1910901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17693989
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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