A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920237



Internal ID22695460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85186673..85186734hg38UCSC Ensembl
chr8:86098908..86098969hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436169
Samples
Known GenesE2F5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920237
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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