A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363382



Internal ID21020935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136116511..136128240hg38UCSC Ensembl
chr3:135835353..135847082hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3811730
hg1911730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094914
Samples
Known GenesPPP2R3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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