A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427329



Internal ID21084882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28568191..28568818hg38UCSC Ensembl
chr8:28425708..28426335hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166158
Samples
Known GenesFZD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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