A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005411



Internal ID7070506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:166856124..166859055hg38UCSC Ensembl
Outerchr5:166283129..166286060hg19UCSC Ensembl
Outerchr5:166215707..166218638hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382932
hg192932
hg182932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564265
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005411
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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