A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375061



Internal ID21032614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8929234..8933291hg38UCSC Ensembl
chr3:8970918..8974975hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg384058
hg194058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104244
Samples
Known GenesRAD18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375061
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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