A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766572



Internal ID20542432
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 StatusM
Merged Variants
Supporting Variantsnssv16265726
Samples
Known GenesSTAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766572
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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