A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479711



Internal ID22537613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83789554..83850636hg38UCSC Ensembl
chr16:83823159..83884241hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3861083
hg1961083
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5867583
Supporting Variants
Samples
Known GenesCDH13, HSBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479711
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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