A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366951



Internal ID21024504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25630901..25632600hg38UCSC Ensembl
chr3:25672392..25674091hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101132
Samples
Known GenesTOP2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366951
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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