A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627983



Internal ID6668127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124613736..124614720hg38UCSC Ensembl
Innerchr11:124613750..124614706hg38UCSC Ensembl
Outerchr11:124613722..124614734hg38UCSC Ensembl
chr11:124483632..124484616hg19UCSC Ensembl
Innerchr11:124483646..124484602hg19UCSC Ensembl
Outerchr11:124483618..124484630hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14302135
SamplesHG04198
Known GenesPANX3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627983
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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