A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364563



Internal ID21022116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8951750..8952182hg38UCSC Ensembl
chr3:8993434..8993866hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104245
Samples
Known GenesRAD18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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