A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726143



Internal ID149809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17773327..17776321hg38UCSC Ensembl
chr21:19145644..19148638hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg382995
hg192995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146571
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726143
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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