A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920443



Internal ID22695666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105480145..105491810hg38UCSC Ensembl
chr8:106492373..106504038hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3811666
hg1911666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439451
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920443
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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