A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902531



Internal ID2502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28516375..28517047hg38UCSC Ensembl
chr1:28842887..28843559hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422790
Supporting Variants
Samples
Known GenesRCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902531
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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