A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892345



Internal ID169091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160983227..160983443hg38UCSC Ensembl
chr1:160953017..160953233hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425768
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892345
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003282


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