A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7130469



Internal ID10408751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:155761728..155761878hg38UCSC Ensembl
Outerchr5:155188738..155188888hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2860902
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7130469
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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