A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372393



Internal ID21029946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184709003..184719614hg38UCSC Ensembl
chr3:184426791..184437402hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3810612
hg1910612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097625
Samples
Known GenesMAGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372393
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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