A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265726



Internal ID20474944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103621311..103621311hg38UCSC Ensembl
chr12:104015089..104015089hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766572
Supporting Variants
Samples
Known GenesSTAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265726
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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