A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3410069



Internal ID15257029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35792197..35799095hg38UCSC Ensembl
Innerchr6:35793197..35798095hg38UCSC Ensembl
Outerchr6:35791197..35800095hg38UCSC Ensembl
chr6:35759974..35766872hg19UCSC Ensembl
Innerchr6:35760974..35765872hg19UCSC Ensembl
Outerchr6:35758974..35767872hg19UCSC Ensembl
chr6:35867952..35874850hg18UCSC Ensembl
Innerchr6:35868952..35873850hg18UCSC Ensembl
Outerchr6:35866952..35875850hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg386899
hg196899
hg186899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3491e59
Supporting Variantsessv8695289
SamplesNA12878
Known GenesCLPS
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3410069
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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