A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952786



Internal ID22728090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125426634..125426634hg38UCSC Ensembl
chr8:126438876..126438876hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952786
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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