A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670892



Internal ID9590311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:27330864..27338761hg38UCSC Ensembl
Outerchr6:27330707..27338914hg38UCSC Ensembl
Innerchr6:27298643..27306540hg19UCSC Ensembl
Outerchr6:27298486..27306693hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg388208
hg198208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6226000
SamplesNA19901
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670892
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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