A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863296



Internal ID22638231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23440533..23446178hg38UCSC Ensembl
chr10:23729462..23735107hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg385646
hg195646
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv153n209
Supporting Variantsnssv17459360
Samples
Known GenesOTUD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863296
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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