A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521083



Internal ID20894444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:44556675..44560448hg38UCSC Ensembl
chr18:42136640..42140413hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg383774
hg193774
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521083
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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