A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610427



Internal ID6650653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114272638..114345103hg38UCSC Ensembl
chr6:114593802..114666267hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3872466
hg1972466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12508951
SamplesNA19092
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610427
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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