A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698702



Internal ID122368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96709020..96709289hg38UCSC Ensembl
chr14:97175357..97175626hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144306
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698702
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.55965


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