A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918636



Internal ID22693858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101423805..101431569hg38UCSC Ensembl
chr11:101294536..101302300hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg387765
hg197765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918636
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