A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271862



Internal ID20481080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125067487..125067487hg38UCSC Ensembl
chr3:124786331..124786331hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271862
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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