A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3574909



Internal ID7046292
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 StateHomozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1010986
Supporting Variants
SamplesHuRef
Known GenesWTAPP1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3574909
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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