A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6518274



Internal ID9002418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:4892208..4893869hg38UCSC Ensembl
Outerchr4:4892051..4894022hg38UCSC Ensembl
Innerchr4:4893935..4895596hg19UCSC Ensembl
Outerchr4:4893778..4895749hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg381972
hg191972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662948
Supporting Variants
SamplesHG00610
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6518274
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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