A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426058



Internal ID21083611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8926433..8943984hg38UCSC Ensembl
chr8:8783943..8801494hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3817552
hg1917552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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