A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9653337



Internal ID13617046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87438802..87438821hg38UCSC Ensembl
Innerchr11:87438798..87438825hg38UCSC Ensembl
Outerchr11:87438779..87438844hg38UCSC Ensembl
chr11:87149844..87149863hg19UCSC Ensembl
Innerchr11:87149840..87149867hg19UCSC Ensembl
Outerchr11:87149821..87149886hg19UCSC Ensembl
chr11:86827492..86827511hg18UCSC Ensembl
Innerchr11:86827515..86827488hg18UCSC Ensembl
Outerchr11:86827469..86827534hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3431247
Supporting Variants
SamplesNA12872
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9653337
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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