A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523372



Internal ID20896733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38630492..38636534hg38UCSC Ensembl
chr20:37259135..37265177hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg386043
hg196043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202247
Samples
Known GenesARHGAP40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523372
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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