A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7738301



Internal ID13167467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34150735..34152468hg38UCSC Ensembl
Outerchr11:34150535..34152668hg38UCSC Ensembl
Innerchr11:34172282..34174015hg19UCSC Ensembl
Outerchr11:34172082..34174215hg19UCSC Ensembl
Innerchr11:34128858..34130591hg18UCSC Ensembl
Outerchr11:34128658..34130791hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382134
hg192134
hg182134
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302725
Supporting Variants
SamplesNA11881
Known GenesABTB2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7738301
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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