A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17726676



Internal ID150342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33625336..33629487hg38UCSC Ensembl
chr21:34997642..35001793hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg384152
hg194152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5548232
Supporting Variants
Samples
Known GenesCRYZL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17726676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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