A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956415



Internal ID22731606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102601986..102601986hg38UCSC Ensembl
chr8:103614214..103614214hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956415
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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