A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915373



Internal ID22690591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85172142..85176012hg38UCSC Ensembl
chr8:86084377..86088247hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg383871
hg193871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915373
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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