A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959754



Internal ID22734776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41888246..41909121hg38UCSC Ensembl
chr21:43308355..43329230hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3820876
hg1920876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17395610
Samples
Known GenesC2CD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959754
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