A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8695281



Internal ID15052237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34276497..34278595hg38UCSC Ensembl
Innerchr6:34277497..34277595hg38UCSC Ensembl
Outerchr6:34275497..34279595hg38UCSC Ensembl
chr6:34244274..34246372hg19UCSC Ensembl
Innerchr6:34245274..34245372hg19UCSC Ensembl
Outerchr6:34243274..34247372hg19UCSC Ensembl
chr6:34352252..34354350hg18UCSC Ensembl
Innerchr6:34353252..34353350hg18UCSC Ensembl
Outerchr6:34351252..34355350hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3377596
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8695281
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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