A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948337



Internal ID22723821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133891172..133891172hg38UCSC Ensembl
chr8:134903415..134903415hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948337
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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