A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734243



Internal ID157909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:19331808..19375808hg38UCSC Ensembl
chr21:20704125..20748125hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3844001
hg1944001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522597
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734243
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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