A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563560



Internal ID6688602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:123558541..123573065hg38UCSC Ensembl
Outerchr11:123429249..123443773hg19UCSC Ensembl
Outerchr11:122934459..122948983hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3814525
hg1914525
hg1814525
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1010432
Supporting Variants
SamplesHuRef
Known GenesGRAMD1B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563560
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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