A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5531914



Internal ID9330622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66513996..66527692hg38UCSC Ensembl
Outerchr4:66513822..66527845hg38UCSC Ensembl
Innerchr4:67379714..67393410hg19UCSC Ensembl
Outerchr4:67379540..67393563hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3814024
hg1914024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673811
Supporting Variants
SamplesNA18526
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5531914
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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