A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5956424



Internal ID22731615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91545757..91545757hg38UCSC Ensembl
chr8:92557985..92557985hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38517
hg19517
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5956424
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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