A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8953795



Internal ID13919982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87438807..87438820hg38UCSC Ensembl
Innerchr11:87438804..87438823hg38UCSC Ensembl
Outerchr11:87438791..87438836hg38UCSC Ensembl
chr11:87149849..87149862hg19UCSC Ensembl
Innerchr11:87149846..87149865hg19UCSC Ensembl
Outerchr11:87149833..87149878hg19UCSC Ensembl
chr11:86827497..86827510hg18UCSC Ensembl
Innerchr11:86827513..86827494hg18UCSC Ensembl
Outerchr11:86827481..86827526hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38287
hg19287
hg18287
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3341248
Supporting Variants
SamplesNA18523
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8953795
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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