A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1006984



Internal ID7072077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:33643375..33646208hg38UCSC Ensembl
Outerchr11:33664921..33667754hg19UCSC Ensembl
Outerchr11:33621497..33624330hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382177
hg192177
hg182177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564328
SamplesHuRef
Known GenesKIAA1549L
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1006984
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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