A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199094



Internal ID20766134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9304841..9315319hg38UCSC Ensembl
chr19:9415517..9425995hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3810479
hg1910479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523763
Supporting Variants
Samples
Known GenesZNF699
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199094
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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