A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289026



Internal ID20498244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102200157..102200157hg38UCSC Ensembl
chr12:102593935..102593935hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38767
hg19767
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289026
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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