A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668211



Internal ID9934316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:123895895..123903206hg38UCSC Ensembl
Outerchr9:123895738..123903359hg38UCSC Ensembl
Innerchr9:126658174..126665485hg19UCSC Ensembl
Outerchr9:126658017..126665638hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg387622
hg197622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5998632
SamplesNA18559
Known GenesDENND1A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668211
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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