A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16894592



Internal ID170563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:198458018..198458096hg38UCSC Ensembl
chr1:198427148..198427226hg19UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451742
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16894592
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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