A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428239



Internal ID21085792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24866152..24876099hg38UCSC Ensembl
chr8:24723665..24733612hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg389948
hg199948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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