A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521060



Internal ID20894421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35675405..35716472hg38UCSC Ensembl
chr19:36166307..36207374hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3841068
hg1941068
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197783
Samples
Known GenesUPK1A, ZBTB32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521060
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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