A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368010



Internal ID21025563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136043258..136047700hg38UCSC Ensembl
chr3:135762100..135766542hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209593
Samples
Known GenesPPP2R3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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