A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265287



Internal ID20474505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176839753..176839753hg38UCSC Ensembl
chr2:177704481..177704481hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265287
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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