A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531565



Internal ID20904926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51768552..52114483hg38UCSC Ensembl
chr19:52271805..52617736hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38345932
hg19345932
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198317
Samples
Known GenesFPR2, FPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF616, ZNF649, ZNF841
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531565
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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