A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424025



Internal ID21081578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24238003..24283012hg38UCSC Ensembl
chr8:24095516..24140525hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3845010
hg1945010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424025
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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