A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660578



Internal ID9579997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21822722..21828303hg38UCSC Ensembl
Outerchr6:21822685..21828353hg38UCSC Ensembl
Innerchr6:21822953..21828534hg19UCSC Ensembl
Outerchr6:21822916..21828584hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385669
hg195669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6068955
SamplesNA18941
Known GenesCASC15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660578
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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