A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532181



Internal ID20905542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35639344..35661087hg38UCSC Ensembl
chr19:36130246..36151989hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3821744
hg1921744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197781
Samples
Known GenesCOX6B1, ETV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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