A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463351



Internal ID21120904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82908332..82920423hg38UCSC Ensembl
chr11:82619374..82631465hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3812092
hg1912092
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184185
Samples
Known GenesC11orf82
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463351
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