A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8647908



Internal ID15147799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85158960..85158960hg38UCSC Ensembl
Innerchr6:85158959..85158961hg38UCSC Ensembl
Outerchr6:85158920..85158980hg38UCSC Ensembl
chr6:85868678..85868678hg19UCSC Ensembl
Innerchr6:85868677..85868679hg19UCSC Ensembl
Outerchr6:85868638..85868698hg19UCSC Ensembl
chr6:85925397..85925397hg18UCSC Ensembl
Innerchr6:85925398..85925396hg18UCSC Ensembl
Outerchr6:85925357..85925417hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3868
hg1968
hg1868
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3435741
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8647908
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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