A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541923



Internal ID20915191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46024145..46029883hg38UCSC Ensembl
chr20:44652784..44658522hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg385739
hg195739
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202904
Samples
Known GenesSLC12A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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