A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272410



Internal ID20481628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106209872..106209872hg38UCSC Ensembl
chr12:106603650..106603650hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4768288
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272410
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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