A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367822



Internal ID21025375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13622007..13627961hg38UCSC Ensembl
chr3:13663507..13669461hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg385955
hg195955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094921
Samples
Known GenesFBLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367822
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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