A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664918



Internal ID9931023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:16334884..16374614hg38UCSC Ensembl
Outerchr4:16334847..16374664hg38UCSC Ensembl
Innerchr4:16336507..16376237hg19UCSC Ensembl
Outerchr4:16336470..16376287hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3839818
hg1939818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5399303
SamplesNA20522
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664918
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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