A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531322



Internal ID20904683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60615131..60787311hg38UCSC Ensembl
chr18:58282364..58454544hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38172181
hg19172181
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185153
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531322
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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