A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665507



Internal ID9931612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24325188..24328044hg38UCSC Ensembl
Outerchr6:24324817..24328414hg38UCSC Ensembl
Innerchr6:24325416..24328272hg19UCSC Ensembl
Outerchr6:24325045..24328642hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg383598
hg193598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1081e199
Supporting Variantsessv6036151, essv6510464, essv5663034, essv6136744, essv5580746, essv5563660, essv5437801, essv6083043, essv6479168, essv6167435
SamplesHG00187, HG00185, HG00277, HG00309, HG00338, HG00328, HG00284, HG00375, HG00342, HG00274
Known GenesDCDC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665507
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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