A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563696



Internal ID7036456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:138611073..138612567hg38UCSC Ensembl
Outerchr7:138295818..138297312hg19UCSC Ensembl
Outerchr7:137946358..137947852hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381495
hg191495
hg181495
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv993410
Supporting Variants
SamplesHuRef
Known GenesSVOPL
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563696
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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