A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457443



Internal ID21114996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102615830..102636011hg38UCSC Ensembl
chr11:102486561..102506742hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3820182
hg1920182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177300
Samples
Known GenesMMP20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457443
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