A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608554



Internal ID21800601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3842987..3845616hg38UCSC Ensembl
chr16:3892988..3895617hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382630
hg192630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6022424
Supporting Variants
Samples
Known GenesCREBBP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608554
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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