A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530747



Internal ID20904108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:64676254..64681090hg38UCSC Ensembl
chr18:62343489..62348325hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg384837
hg194837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530747
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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