A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420643



Internal ID21078196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67633001..67642200hg38UCSC Ensembl
chr8:68545236..68554435hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170548
Samples
Known GenesCPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420643
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