A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916447



Internal ID22691666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96414841..96418299hg38UCSC Ensembl
chr8:97427069..97430527hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg383459
hg193459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916447
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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