A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529657



Internal ID20903018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38785830..38791247hg38UCSC Ensembl
chr20:37414473..37419890hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg385418
hg195418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529657
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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