A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519716



Internal ID20893077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:776008..779855hg38UCSC Ensembl
chr20:756651..760498hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383848
hg193848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519716
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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