A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563567



Internal ID6688609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:57640821..57651878hg38UCSC Ensembl
Outerchr11:57408294..57419351hg19UCSC Ensembl
Outerchr11:57164870..57175927hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811058
hg1911058
hg1811058
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992553
Supporting Variants
SamplesHuRef
Known GenesMIR130A, YPEL4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563567
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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