A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666111



Internal ID9585530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:9879442..9888353hg38UCSC Ensembl
Outerchr3:9879405..9888403hg38UCSC Ensembl
Innerchr3:9921126..9930037hg19UCSC Ensembl
Outerchr3:9921089..9930087hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg388999
hg198999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5856847, essv5821446, essv6145166
SamplesHG00536, HG00449, NA18973
Known GenesCIDEC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666111
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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