A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17720020



Internal ID143686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:221000..338000hg38UCSC Ensembl
chr19:221000..338000hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38117001
hg19117001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145483
Supporting Variants
Samples
Known GenesMIER2, PPAP2C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17720020
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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