A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276117



Internal ID20485335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112732378..112732378hg38UCSC Ensembl
chr2:113489955..113489955hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276117
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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