A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664898



Internal ID9931003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43264827..43272501hg38UCSC Ensembl
Outerchr4:43264790..43272551hg38UCSC Ensembl
Innerchr4:43266844..43274518hg19UCSC Ensembl
Outerchr4:43266807..43274568hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg387762
hg197762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6559121
SamplesNA18638
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664898
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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