A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523477



Internal ID20896838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21901131..21902664hg38UCSC Ensembl
chr20:21881769..21883302hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg381534
hg191534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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