A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466184



Internal ID21123737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41583695..41682088hg38UCSC Ensembl
chr11:41605245..41703638hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3898394
hg1998394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466184
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