A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17722072



Internal ID145738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19045667..19046281hg38UCSC Ensembl
chr19:19156476..19157090hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531328
Supporting Variants
Samples
Known GenesARMC6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17722072
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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