A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726701



Internal ID150367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35525445..35525637hg38UCSC Ensembl
chr21:36897743..36897935hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551810
Supporting Variants
Samples
Known GenesLOC100506403
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726701
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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