A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533619



Internal ID20906980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46332701..46335800hg38UCSC Ensembl
chr18:43912664..43915763hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178985
Samples
Known GenesRNF165
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533619
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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