A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362012



Internal ID21019565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107403876..107406349hg38UCSC Ensembl
chr3:107122723..107125196hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg382474
hg192474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362012
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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