A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423537



Internal ID21081090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33259211..33259805hg38UCSC Ensembl
chr8:33116729..33117323hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer