A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8927975



Internal ID14076615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13718233..13718246hg38UCSC Ensembl
Innerchr6:13718223..13718254hg38UCSC Ensembl
Outerchr6:13718210..13718267hg38UCSC Ensembl
chr6:13718465..13718478hg19UCSC Ensembl
Innerchr6:13718455..13718486hg19UCSC Ensembl
Outerchr6:13718442..13718499hg19UCSC Ensembl
chr6:13826444..13826457hg18UCSC Ensembl
Innerchr6:13826465..13826434hg18UCSC Ensembl
Outerchr6:13826421..13826478hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38270
hg19270
hg18270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3436267
Supporting Variants
SamplesNA18561
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8927975
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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