A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422057



Internal ID21079610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:136385130..136425651hg38UCSC Ensembl
chr8:137397373..137437894hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3840522
hg1940522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422057
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