A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533280



Internal ID20906641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:49497599..49504590hg38UCSC Ensembl
chr18:47023969..47030960hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg386992
hg196992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533280
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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