A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423613



Internal ID21081166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23267868..23268252hg38UCSC Ensembl
chr8:23125381..23125765hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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