A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5786647



Internal ID8764050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3627786..3630092hg38UCSC Ensembl
Outerchr11:3627415..3630462hg38UCSC Ensembl
Innerchr11:3649016..3651322hg19UCSC Ensembl
Outerchr11:3648645..3651692hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383048
hg193048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657153
Supporting Variants
SamplesHG00578
Known GenesTRPC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5786647
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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