A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503795



Internal ID20877051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80697204..80699263hg38UCSC Ensembl
chr16:80731101..80733160hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg382060
hg192060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032290
Samples
Known GenesCDYL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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