A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083738



Internal ID21992971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:89543830..89543830hg38UCSC Ensembl
chr12:89937607..89937607hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602354
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083738
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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