A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530179



Internal ID20903540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22619448..22620839hg38UCSC Ensembl
chr20:22600086..22601477hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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