A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726349



Internal ID150015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:24612372..24660556hg38UCSC Ensembl
chr21:25984686..26032870hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3848185
hg1948185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726349
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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