A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14486306



Internal ID3184578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55656445..55668301hg38UCSC Ensembl
chr12:56050229..56062085hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3811857
hg1911857
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3629585
Supporting Variants
SamplesHG02799
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14486306
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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