A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711459



Internal ID135125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11882731..11882801hg38UCSC Ensembl
chr17:11786048..11786118hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521514
Supporting Variants
Samples
Known GenesDNAH9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711459
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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