A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876884



Internal ID22651846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66010803..66027110hg38UCSC Ensembl
chr17:64006921..64023228hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3816308
hg1916308
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475812
Samples
Known GenesCEP112
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876884
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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