A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040030



Internal ID21949373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109661276..109662019hg38UCSC Ensembl
chr12:110099081..110099824hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040030
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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