A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3629078



Internal ID6669218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32419473..32449857hg38UCSC Ensembl
chr12:32572407..32602791hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3830385
hg1930385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv265e214
Supporting Variantsessv14438224
SamplesHG02464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3629078
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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