A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363344



Internal ID21020897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:19983801..19985400hg38UCSC Ensembl
chr3:20025293..20026892hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101294
Samples
Known GenesPP2D1, RAB5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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