A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428515



Internal ID21086068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:71336072..71346093hg38UCSC Ensembl
chr8:72248307..72258328hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3810022
hg1910022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169619
Samples
Known GenesEYA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428515
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