A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003572



Internal ID6715701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:61677768..61689740hg38UCSC Ensembl
Outerchr11:61445240..61457212hg19UCSC Ensembl
Outerchr11:61201816..61213788hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3811973
hg1911973
hg1811973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564710
SamplesHuRef
Known GenesDAGLA
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003572
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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