A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628033



Internal ID21820080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31055661..31065870hg38UCSC Ensembl
chr16:31066982..31077191hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3810210
hg1910210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027954
Supporting Variants
Samples
Known GenesZNF668
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628033
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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