A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468929



Internal ID21126482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63370321..63370941hg38UCSC Ensembl
chr11:63137793..63138413hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993787
Samples
Known GenesMIR3680-1, MIR3680-2, SLC22A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer