A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284392



Internal ID20493610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:56669882..56669882hg38UCSC Ensembl
chr15:56962080..56962080hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761670
Supporting Variants
Samples
Known GenesZNF280D
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284392
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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