A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8951572



Internal ID13883614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13922584..13922628hg38UCSC Ensembl
Innerchr11:13922600..13922609hg38UCSC Ensembl
Outerchr11:13922556..13922656hg38UCSC Ensembl
chr11:13944131..13944175hg19UCSC Ensembl
Innerchr11:13944147..13944156hg19UCSC Ensembl
Outerchr11:13944103..13944203hg19UCSC Ensembl
chr11:13900707..13900751hg18UCSC Ensembl
Innerchr11:13900732..13900723hg18UCSC Ensembl
Outerchr11:13900679..13900779hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg385988
hg195988
hg185988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3342687
Supporting Variants
SamplesNA18519
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8951572
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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