A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523836



Internal ID20897197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5041982..5047246hg38UCSC Ensembl
chr20:5022628..5027892hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385265
hg195265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523836
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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