A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029302



Internal ID21938645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109841044..109843118hg38UCSC Ensembl
chr12:110278849..110280923hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382075
hg192075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029302
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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