A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924580



Internal ID22699807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80380746..80393695hg38UCSC Ensembl
chr8:81292981..81305930hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3812950
hg1912950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441952
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924580
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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