A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900821



Internal ID22675968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218710874..218710927hg38UCSC Ensembl
chr2:219575597..219575650hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17399956
Samples
Known GenesTTLL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900821
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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