A curated catalogue of human genomic structural variation




Variant Details

Variant: esv260008



Internal ID1801748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161149409..161149410hg19UCSC Ensembl
Outerchr6:161149283..161149537hg19UCSC Ensembl
Innerchr6:161069400..161069399hg18UCSC Ensembl
Outerchr6:161069273..161069527hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeOTHER Complex
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv2396502, essv2399431, essv2397280, essv2399519, essv2399682, essv2396944, essv2394740, essv2400468, essv2396380, essv2400416, essv2397095, essv2395970
SamplesNA19137, NA18517, NA19210, NA19239, NA07357, NA18592, NA12892, NA19238, NA18858, NA19138, NA12878, NA19240
Known GenesPLG
Method
AnalysisAnalysis structural variant merging of all supporting structural variant calls generated by type of computational approach: read pair mapping.
PlatformIllumina Genome Analyzer II
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv260008
Frequency
Sample Size157
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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