A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661942



Internal ID9928047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66873289..66891702hg38UCSC Ensembl
Outerchr7:66873252..66891752hg38UCSC Ensembl
Innerchr7:66338276..66356689hg19UCSC Ensembl
Outerchr7:66338239..66356739hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3818501
hg1918501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5987621, essv6420065
SamplesNA12341, NA12777
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661942
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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