A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669102



Internal ID9935207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:165813167..165817660hg38UCSC Ensembl
Outerchr2:165813130..165817710hg38UCSC Ensembl
Innerchr2:166669677..166674170hg19UCSC Ensembl
Outerchr2:166669640..166674220hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg384581
hg194581
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv745e199
Supporting Variantsessv6162795
SamplesNA18622
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669102
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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