A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533912



Internal ID20907273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33185620..33195002hg38UCSC Ensembl
chr20:31773426..31782808hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg389383
hg199383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067433
Samples
Known GenesBPIFA4P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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