A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628236



Internal ID6668379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:417352..561839hg38UCSC Ensembl
chr12:526518..671005hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38144488
hg19144488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14329576, essv14329575, essv14329574
SamplesNA19435, HG03836, NA19403
Known GenesB4GALNT3, CCDC77
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628236
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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