A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197783



Internal ID20764823
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 StatusS
Merged Variantsnsv6521060
Supporting Variants
Samples
Known GenesUPK1A, ZBTB32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197783
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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