A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530709



Internal ID20904070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11333103..11334172hg38UCSC Ensembl
chr20:11313751..11314820hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381070
hg191070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530709
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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