A curated catalogue of human genomic structural variation




Variant Details

Variant: esv990812



Internal ID6726778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14326766..14327081hg38UCSC Ensembl
chr11:14348312..14348627hg19UCSC Ensembl
chr11:14304888..14305203hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38316
hg19316
hg18316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3572440
SamplesHuRef
Known GenesRRAS2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv990812
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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