A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv21n199



Internal ID22802907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13392585..13400418hg38UCSC Ensembl
chr12:13545519..13553352hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg387834
hg197834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4742771, nsv4732875
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv21n199
Frequency
Sample Size25
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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