A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1004097



Internal ID7069199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:138044874..138046280hg38UCSC Ensembl
Outerchr4:138966028..138967434hg19UCSC Ensembl
Outerchr4:139185478..139186884hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg381407
hg191407
hg181407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv127e180
Supporting Variantsessv3564290
SamplesHuRef
Known GenesLINC00616
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1004097
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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