A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959939



Internal ID22734958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132510317..132510317hg38UCSC Ensembl
chr8:133522564..133522564hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959939
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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