A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895233



Internal ID171000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202845822..202845881hg38UCSC Ensembl
chr1:202814950..202815009hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895233
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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