A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3352859



Internal ID15199840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13714641..13715739hg38UCSC Ensembl
Innerchr6:13714739..13715641hg38UCSC Ensembl
Outerchr6:13713641..13716739hg38UCSC Ensembl
chr6:13714873..13715971hg19UCSC Ensembl
Innerchr6:13714971..13715873hg19UCSC Ensembl
Outerchr6:13713873..13716971hg19UCSC Ensembl
chr6:13822852..13823950hg18UCSC Ensembl
Innerchr6:13823852..13822950hg18UCSC Ensembl
Outerchr6:13821852..13824950hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695047
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3352859
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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