A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733881



Internal ID157547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9817869..9820584hg38UCSC Ensembl
chr4_gl000193_random:85183..87898hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382716
hg192716
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517587
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733881
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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