A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662919



Internal ID9929024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:84538653..84542362hg38UCSC Ensembl
Outerchr4:84538496..84542515hg38UCSC Ensembl
Innerchr4:85459806..85463515hg19UCSC Ensembl
Outerchr4:85459649..85463668hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg384020
hg194020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv959e199
Supporting Variantsessv6119307
SamplesNA12155
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662919
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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