A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16279541



Internal ID20488759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172411418..172411418hg38UCSC Ensembl
chr2:173276146..173276146hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759209
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16279541
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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