A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698652



Internal ID122318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95668039..95678463hg38UCSC Ensembl
chr14:96134376..96144800hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3810425
hg1910425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495938
Supporting Variants
Samples
Known GenesTCL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698652
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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