A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007428



Internal ID7072522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154660106..154664256hg38UCSC Ensembl
Innerchr7:154451816..154455966hg19UCSC Ensembl
Innerchr7:154082749..154086899hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg384151
hg194151
hg184151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586567
SamplesHuRef
Known GenesDPP6
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007428
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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