A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910721



Internal ID22685932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68844797..68847443hg38UCSC Ensembl
chr10:70604553..70607199hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382647
hg192647
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360891
Samples
Known GenesSTOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910721
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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