A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528602



Internal ID20901963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32734390..32742387hg38UCSC Ensembl
chr20:31322197..31330193hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg387998
hg197997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203278
Samples
Known GenesCOMMD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528602
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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