A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2861569



Internal ID10881266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:178005724..178006241hg38UCSC Ensembl
Outerchr4:178926878..178927395hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7131136
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2861569
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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