A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275294



Internal ID20484512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169167966..169167966hg38UCSC Ensembl
chr3:168885754..168885754hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765708
Supporting Variants
Samples
Known GenesMECOM
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275294
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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