A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720626



Internal ID144292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3901779..3932372hg38UCSC Ensembl
chr19:3901777..3932370hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3830594
hg1930594
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521920
Supporting Variants
Samples
Known GenesATCAY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720626
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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