A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3364588



Internal ID15211566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94640025..94640025hg38UCSC Ensembl
Innerchr11:94640024..94640026hg38UCSC Ensembl
Outerchr11:94639975..94640075hg38UCSC Ensembl
chr11:94373191..94373191hg19UCSC Ensembl
Innerchr11:94373190..94373192hg19UCSC Ensembl
Outerchr11:94373141..94373241hg19UCSC Ensembl
chr11:94012839..94012839hg18UCSC Ensembl
Innerchr11:94012840..94012838hg18UCSC Ensembl
Outerchr11:94012789..94012889hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38128
hg19128
hg18128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8653065, essv8653063, essv8653066
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3364588
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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