A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3387730



Internal ID15234699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32412722..32412741hg38UCSC Ensembl
Innerchr11:32412718..32412745hg38UCSC Ensembl
Outerchr11:32412699..32412764hg38UCSC Ensembl
chr11:32434268..32434287hg19UCSC Ensembl
Innerchr11:32434264..32434291hg19UCSC Ensembl
Outerchr11:32434245..32434310hg19UCSC Ensembl
chr11:32390844..32390863hg18UCSC Ensembl
Innerchr11:32390867..32390840hg18UCSC Ensembl
Outerchr11:32390821..32390886hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9651802, essv9651813, essv9651791, essv9651757, essv9651746, essv9651768, essv9651780
SamplesNA18969, NA07346, NA12287, NA12815, NA12872, NA12249, NA12874
Known GenesWT1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3387730
Frequency
Sample Size185
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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