A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522316



Internal ID20895677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7445479..7457184hg38UCSC Ensembl
chr20:7426126..7437831hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3811706
hg1911706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522316
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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