A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366108



Internal ID21023661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96605055..96625207hg38UCSC Ensembl
chr3:96323899..96344051hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3820153
hg1920153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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