A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460059



Internal ID21117612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:86396246..86396942hg38UCSC Ensembl
chr12:86790024..86790720hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005451
Samples
Known GenesMGAT4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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