A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660764



Internal ID9926869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31838548..31838954hg38UCSC Ensembl
Outerchr11:31838391..31839107hg38UCSC Ensembl
Innerchr11:31860095..31860501hg19UCSC Ensembl
Outerchr11:31859938..31860654hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5439763, essv6504862, essv6027288, essv6153986, essv5674908
SamplesHG01462, HG01188, NA19982, NA18910, NA19147
Known GenesDKFZp686K1684
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660764
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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