A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865469



Internal ID13317832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33937948..33937948hg38UCSC Ensembl
Innerchr11:33937946..33937950hg38UCSC Ensembl
Outerchr11:33937946..33937950hg38UCSC Ensembl
chr11:33959495..33959495hg19UCSC Ensembl
Innerchr11:33959493..33959497hg19UCSC Ensembl
Outerchr11:33959493..33959497hg19UCSC Ensembl
chr11:33916071..33916071hg18UCSC Ensembl
Innerchr11:33916073..33916069hg18UCSC Ensembl
Outerchr11:33916069..33916073hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3858
hg1958
hg1858
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3386259
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865469
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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