A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290115



Internal ID20499333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64315004..64315004hg38UCSC Ensembl
chr3:64300680..64300680hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290115
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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