A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666017



Internal ID9932122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92773637..92784218hg38UCSC Ensembl
Outerchr9:92773600..92784268hg38UCSC Ensembl
Innerchr9:95535919..95546500hg19UCSC Ensembl
Outerchr9:95535882..95546550hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3810669
hg1910669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6388150
SamplesHG01366
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666017
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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