A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3448441



Internal ID15295390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106011684..106012682hg38UCSC Ensembl
Innerchr6:106011683..106012683hg38UCSC Ensembl
Outerchr6:106010684..106013682hg38UCSC Ensembl
chr6:106459559..106460557hg19UCSC Ensembl
Innerchr6:106459558..106460558hg19UCSC Ensembl
Outerchr6:106458559..106461557hg19UCSC Ensembl
chr6:106566252..106567250hg18UCSC Ensembl
Innerchr6:106567251..106566251hg18UCSC Ensembl
Outerchr6:106565252..106568250hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695012
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3448441
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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