A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880025



Internal ID22654995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65916438..65919709hg38UCSC Ensembl
chr17:63912556..63915827hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg383272
hg193272
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475811
Samples
Known GenesCEP112
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880025
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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