A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469907



Internal ID21127460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123134396..123910360hg38UCSC Ensembl
chr11:123005104..123781067hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38775965
hg19775964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195472
Samples
Known GenesCLMP, GRAMD1B, MIR4493, OR6M1, OR6X1, OR8D4, SCN3B, TMEM225, ZNF202
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469907
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