A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024698



Internal ID84198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36820871..36824874hg38UCSC Ensembl
chr9:36820868..36824871hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg384004
hg194004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493384
Supporting Variants
Samples
Known GenesMIR4475
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024698
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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