A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670388



Internal ID9936493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19530987..19537603hg38UCSC Ensembl
Outerchr6:19530950..19537653hg38UCSC Ensembl
Innerchr6:19531218..19537834hg19UCSC Ensembl
Outerchr6:19531181..19537884hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386704
hg196704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5652462
SamplesNA18605
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670388
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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