A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424926



Internal ID21082479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128672161..128672830hg38UCSC Ensembl
chr8:129684407..129685076hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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