A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850623



Internal ID22625558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23441483..23445728hg38UCSC Ensembl
chr10:23730412..23734657hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384246
hg194246
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv153n209
Supporting Variantsnssv17464129
Samples
Known GenesOTUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850623
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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