A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033882



Internal ID21943225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:86296032..86296150hg38UCSC Ensembl
chr12:86689810..86689928hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609566
Samples
Known GenesMGAT4C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033882
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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