A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16905971



Internal ID4779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91229521..91229621hg38UCSC Ensembl
chr1:91695078..91695178hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16905971
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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