A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532964



Internal ID20906325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10792961..10794491hg38UCSC Ensembl
chr20:10773609..10775139hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381531
hg191531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066251
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532964
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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