A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910207



Internal ID22685417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74074436..74091104hg38UCSC Ensembl
chr8:74986671..75003339hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3816669
hg1916669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910207
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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