A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661623



Internal ID9927728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:53613762..53615718hg38UCSC Ensembl
Outerchr6:53613605..53615871hg38UCSC Ensembl
Innerchr6:53478560..53480516hg19UCSC Ensembl
Outerchr6:53478403..53480669hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg382267
hg192267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6058105
SamplesHG00111
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661623
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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