A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037772



Internal ID21947115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:86296121..86296238hg38UCSC Ensembl
chr12:86689899..86690016hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611017
Samples
Known GenesMGAT4C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037772
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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