A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408766



Internal ID21066319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29574703..29588778hg38UCSC Ensembl
chr6:29542480..29556555hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3814076
hg1914076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141365
Samples
Known GenesOR2H2, SNORD32B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408766
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