A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891969



Internal ID168839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174061299..174094656hg38UCSC Ensembl
chr1:174030437..174063794hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3833358
hg1933358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431319
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891969
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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