A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292670



Internal ID20501888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4017065..4017546hg38UCSC Ensembl
chr16:4067066..4067547hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731985
Supporting Variants
Samples
Known GenesADCY9
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292670
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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