A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479710



Internal ID22537612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83789485..83803333hg38UCSC Ensembl
chr16:83823090..83836938hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3813849
hg1913849
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5869308
Supporting Variants
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479710
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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