A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850894



Internal ID22625829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56837910..56839156hg38UCSC Ensembl
chr14:57304628..57305874hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461931
Samples
Known GenesOTX2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850894
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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