A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525083



Internal ID20898444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45126017..45150824hg38UCSC Ensembl
chr18:42705982..42730789hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3824808
hg1924808
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195042
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525083
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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