A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452447



Internal ID21110000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18132444..18140753hg38UCSC Ensembl
chr11:18153991..18162300hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg388310
hg198310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988631
Samples
Known GenesMRGPRX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452447
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