A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16894752



Internal ID170670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205136935..205137293hg38UCSC Ensembl
chr1:205106063..205106421hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38359
hg19359
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5442360
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16894752
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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