A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17732209



Internal ID155875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36595566..36596967hg38UCSC Ensembl
chr20:35223969..35225370hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516639
Supporting Variants
Samples
Known GenesTGIF2-C20orf24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17732209
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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