A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434357



Internal ID15281311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169313532..169316230hg38UCSC Ensembl
Innerchr6:169314532..169315230hg38UCSC Ensembl
Outerchr6:169312532..169317230hg38UCSC Ensembl
chr6:169713627..169716325hg19UCSC Ensembl
Innerchr6:169714627..169715325hg19UCSC Ensembl
Outerchr6:169712627..169717325hg19UCSC Ensembl
chr6:169455552..169458250hg18UCSC Ensembl
Innerchr6:169456552..169457250hg18UCSC Ensembl
Outerchr6:169454552..169459250hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695134
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434357
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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