A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469555



Internal ID21127108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62636580..62640261hg38UCSC Ensembl
chr11:62404052..62407733hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg383682
hg193682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993217
Samples
Known GenesGANAB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469555
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