A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533687



Internal ID20907048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37910595..37910993hg38UCSC Ensembl
chr18:35490559..35490957hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533687
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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