A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452104



Internal ID21109657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112994003..112995049hg38UCSC Ensembl
chr10:114753762..114754808hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg381047
hg191047
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184194
Samples
Known GenesTCF7L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452104
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