A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3334474



Internal ID15181463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130888725..130888741hg38UCSC Ensembl
Innerchr11:130888725..130888739hg38UCSC Ensembl
Outerchr11:130888711..130888755hg38UCSC Ensembl
chr11:130758620..130758636hg19UCSC Ensembl
Innerchr11:130758620..130758634hg19UCSC Ensembl
Outerchr11:130758606..130758650hg19UCSC Ensembl
chr11:130263830..130263846hg18UCSC Ensembl
Innerchr11:130263844..130263830hg18UCSC Ensembl
Outerchr11:130263816..130263860hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381611
hg191611
hg181611
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8672001
SamplesNA19239
Known GenesSNX19
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3334474
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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