A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17475812



Internal ID22533710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66010803..66027110hg38UCSC Ensembl
chr17:64006921..64023228hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg3816308
hg1916308
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876884
Supporting Variants
Samples
Known GenesCEP112
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17475812
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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