A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530861



Internal ID20904222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23849629..23872368hg38UCSC Ensembl
chr20:23830266..23853005hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3822740
hg1922740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203242
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530861
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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