A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453076



Internal ID21110629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20437796..20442196hg38UCSC Ensembl
chr11:20459342..20463742hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384401
hg194401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989194
Samples
Known GenesPRMT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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