A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17459360



Internal ID22517243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23440533..23446178hg38UCSC Ensembl
chr10:23729462..23735107hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg385646
hg195646
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863296
Supporting Variants
Samples
Known GenesOTUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17459360
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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