A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1361n223



Internal ID22804329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7768134..7793845hg38UCSC Ensembl
chr12:7920730..7946441hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3825712
hg1925712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6473551, nsv6472073
Samples
Known GenesNANOG, NANOGNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1361n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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