A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661576



Internal ID9927681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85449755..85475527hg38UCSC Ensembl
Outerchr7:85449711..85475577hg38UCSC Ensembl
Innerchr7:85079071..85104843hg19UCSC Ensembl
Outerchr7:85079027..85104893hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3825867
hg1925867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5565772
SamplesHG01198
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661576
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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