A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364521



Internal ID21022074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43375038..43375365hg38UCSC Ensembl
chr3:43416530..43416857hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099953
Samples
Known GenesANO10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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