A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669045



Internal ID9588464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103000813..103060880hg38UCSC Ensembl
Outerchr9:103000776..103060930hg38UCSC Ensembl
Innerchr9:105763095..105823162hg19UCSC Ensembl
Outerchr9:105763058..105823212hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3860155
hg1960155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1363e199
Supporting Variantsessv6266098
SamplesHG00375
Known GenesCYLC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669045
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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