A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533655



Internal ID20907016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9679979..9749303hg38UCSC Ensembl
chr19:9790655..9859979hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3869325
hg1969325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199097
Samples
Known GenesZNF812
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533655
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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