A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714187



Internal ID137853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67819554..67821082hg38UCSC Ensembl
chr17:65815670..65817198hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg381529
hg191529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521346
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714187
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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