A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564057



Internal ID6688440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:94128771..94139746hg38UCSC Ensembl
Outerchr11:93861937..93872912hg19UCSC Ensembl
Outerchr11:93501585..93512560hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3810976
hg1910976
hg1810976
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989619
Supporting Variants
SamplesHuRef
Known GenesPANX1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564057
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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