A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029756



Internal ID21939099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12253264..12254142hg38UCSC Ensembl
chr12:12406198..12407076hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614871
Samples
Known GenesLRP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029756
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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