A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924103



Internal ID22699330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23441498..23445926hg38UCSC Ensembl
chr10:23730427..23734855hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384429
hg194429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350849
Samples
Known GenesOTUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924103
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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