A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515557



Internal ID292039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51768552..52114487hg38UCSC Ensembl
chr19:52271805..52617740hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38345936
hg19345936
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724134
Samples
Known GenesFPR2, FPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF616, ZNF649, ZNF841
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515557
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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