A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900142



Internal ID880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23380747..23380806hg38UCSC Ensembl
chr1:23707240..23707299hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430733
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900142
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01


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