A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960380



Internal ID22735359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91066603..91066603hg38UCSC Ensembl
chr8:92078831..92078831hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960380
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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