A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010986



Internal ID7074937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102828854..102828915hg38UCSC Ensembl
chr11:102699585..102699646hg19UCSC Ensembl
chr11:102204795..102204856hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3862
hg1962
hg1862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3574909
SamplesHuRef
Known GenesWTAPP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010986
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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