A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17714055



Internal ID137721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:64224999..64226880hg38UCSC Ensembl
chr17:62302359..62304240hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381882
hg191882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525109
Supporting Variants
Samples
Known GenesTEX2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17714055
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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