A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663904



Internal ID9930009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:70347019..70347516hg38UCSC Ensembl
Outerchr6:70346982..70347566hg38UCSC Ensembl
Innerchr6:71056722..71057219hg19UCSC Ensembl
Outerchr6:71056685..71057269hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5410174
SamplesNA18517
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663904
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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