A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090870



Internal ID22000103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78588776..78588776hg38UCSC Ensembl
chr12:78982556..78982556hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600972
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090870
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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