A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430874



Internal ID21088427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113010301..113033000hg38UCSC Ensembl
chr8:114022530..114045229hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3822700
hg1922700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7464n223
Supporting Variantsnssv18220222
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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