A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448539



Internal ID21106092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44861389..44883076hg38UCSC Ensembl
chr10:45356837..45378524hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3821688
hg1921688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194031
Samples
Known GenesTMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448539
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