A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17696729



Internal ID120395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64373557..64380465hg38UCSC Ensembl
chr14:64840275..64847183hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg386909
hg196909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495914
Supporting Variants
Samples
Known GenesMIR548AZ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17696729
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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