A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8952919



Internal ID12972969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43335381..43335403hg38UCSC Ensembl
Innerchr11:43335385..43335397hg38UCSC Ensembl
Outerchr11:43335365..43335419hg38UCSC Ensembl
chr11:43356931..43356953hg19UCSC Ensembl
Innerchr11:43356935..43356947hg19UCSC Ensembl
Outerchr11:43356915..43356969hg19UCSC Ensembl
chr11:43313507..43313529hg18UCSC Ensembl
Innerchr11:43313523..43313511hg18UCSC Ensembl
Outerchr11:43313491..43313545hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38166
hg19166
hg18166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3355802
Supporting Variants
SamplesNA12006
Known GenesAPI5
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8952919
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer