A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464129



Internal ID22522015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23441483..23445728hg38UCSC Ensembl
chr10:23730412..23734657hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg384246
hg194246
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850623
Supporting Variants
Samples
Known GenesOTUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464129
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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