A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433260



Internal ID21090813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86104040..86119503hg38UCSC Ensembl
chr8:87116269..87131732hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3815464
hg1915464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236392
Samples
Known GenesATP6V0D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433260
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