A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675052



Internal ID9941157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122085349..122087069hg38UCSC Ensembl
Outerchr9:122085312..122087119hg38UCSC Ensembl
Innerchr9:124847628..124849348hg19UCSC Ensembl
Outerchr9:124847591..124849398hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381808
hg191808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6465986
SamplesHG00657
Known GenesTTLL11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675052
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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