A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666050



Internal ID9932155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103566410..103569421hg38UCSC Ensembl
Outerchr9:103566376..103569456hg38UCSC Ensembl
Innerchr9:106328692..106331703hg19UCSC Ensembl
Outerchr9:106328658..106331738hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg383081
hg193081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5921354
SamplesHG01191
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666050
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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