A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521035



Internal ID20894396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76563291..76861516hg38UCSC Ensembl
chr18:74275248..74573472hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38298226
hg19298225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197211
Samples
Known GenesLOC100131655, ZNF236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521035
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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