A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614528



Internal ID21806575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3741662..3741662hg38UCSC Ensembl
chr16:3791663..3791663hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097658
Supporting Variants
Samples
Known GenesCREBBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614528
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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