A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909210



Internal ID22684420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90056945..90057266hg38UCSC Ensembl
chr8:91069173..91069494hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909210
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