A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911137



Internal ID22686350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89994288..89994344hg38UCSC Ensembl
chr8:91006516..91006572hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445096
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911137
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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