A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010796



Internal ID7074747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:13882729..13885840hg38UCSC Ensembl
Outerchr11:13904276..13907387hg19UCSC Ensembl
Outerchr11:13860852..13863963hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg383112
hg193112
hg183112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564949
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010796
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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