A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364783



Internal ID21022336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106267359..106267767hg38UCSC Ensembl
chr3:105986206..105986614hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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