A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362052



Internal ID21019605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133640177..133642543hg38UCSC Ensembl
chr3:133359021..133361387hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382367
hg192367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094802
Samples
Known GenesTOPBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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