A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16908048



Internal ID6153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110552909..110552968hg38UCSC Ensembl
chr1:111095531..111095590hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16908048
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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