A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711895



Internal ID135561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18272108..18274235hg38UCSC Ensembl
chr17:18175422..18177549hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382128
hg192128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528322
Supporting Variants
Samples
Known GenesTOP3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711895
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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