A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998925



Internal ID6734856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55317289..55429002hg38UCSC Ensembl
chr11:55084765..55196478hg19UCSC Ensembl
chr11:54841341..54953054hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38111714
hg19111714
hg18111714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3570470
SamplesHuRef
Known GenesOR4A15, OR4A16
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998925
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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