A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468014



Internal ID21125567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50804801..50821400hg38UCSC Ensembl
chr11:50763972..50780519hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3816600
hg1916548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468014
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