A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531208



Internal ID20904569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:48899307..48903714hg38UCSC Ensembl
chr18:46425677..46430084hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg384408
hg194408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531208
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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