A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759209



Internal ID20535069
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 StatusM
Merged Variants
Supporting Variantsnssv16279541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759209
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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