A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6381331



Internal ID21038884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11834772..11838450hg38UCSC Ensembl
chr5:11834884..11838562hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg383679
hg193679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122969
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6381331
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