A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17017739



Internal ID79476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:886291..890775hg38UCSC Ensembl
chr9:886291..890775hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg384485
hg194485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478329
Supporting Variants
Samples
Known GenesDMRT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17017739
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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