A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3630628



Internal ID7017444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104196087..104205750hg38UCSC Ensembl
chr12:104589865..104599528hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg389664
hg199664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv300e214
Supporting Variantsessv14596811, essv14596812
SamplesNA20894, HG01976
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3630628
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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