A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411976



Internal ID21069529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65114322..65210553hg38UCSC Ensembl
chr6:65824215..65920446hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3896232
hg1996232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145692
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411976
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