A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465044



Internal ID21122597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61435852..61458449hg38UCSC Ensembl
chr11:61203324..61225921hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3822598
hg1922598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185965
Samples
Known GenesSDHAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465044
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer