A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711898



Internal ID135564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18309650..18309723hg38UCSC Ensembl
chr17:18212964..18213037hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5532194
Supporting Variants
Samples
Known GenesTOP3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711898
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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