A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282674



Internal ID20491892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51834016..51834016hg38UCSC Ensembl
chr12:52227800..52227800hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282674
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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