A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714053



Internal ID137719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64218502..64227776hg38UCSC Ensembl
chr17:62295862..62305136hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg389275
hg199275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531450
Supporting Variants
Samples
Known GenesTEX2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714053
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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