A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922010



Internal ID22697234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86128277..86156834hg38UCSC Ensembl
chr8:87140506..87169063hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3828558
hg1928558
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432786
Samples
Known GenesATP6V0D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922010
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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