A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891893



Internal ID168790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169495107..169495195hg38UCSC Ensembl
chr1:169464345..169464433hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891893
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.046051


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