A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370009



Internal ID22595678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2434355..2434994hg38UCSC Ensembl
chr16:2484356..2484995hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935847
Supporting Variants
Samples
Known GenesCCNF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370009
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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