A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8695066



Internal ID15050527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156370126..156372224hg38UCSC Ensembl
Innerchr6:156371126..156371224hg38UCSC Ensembl
Outerchr6:156369126..156373224hg38UCSC Ensembl
chr6:156691260..156693358hg19UCSC Ensembl
Innerchr6:156692260..156692358hg19UCSC Ensembl
Outerchr6:156690260..156694358hg19UCSC Ensembl
chr6:156732952..156735050hg18UCSC Ensembl
Innerchr6:156733952..156734050hg18UCSC Ensembl
Outerchr6:156731952..156736050hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382099
hg192099
hg182099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3398871
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8695066
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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