A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9651768



Internal ID13425113
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 StatusS
Merged Variantsesv3387730
Supporting Variants
SamplesNA12249
Known GenesWT1
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9651768
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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