A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627142



Internal ID7013972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88054222..88097170hg38UCSC Ensembl
chr11:87787390..87830338hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3842949
hg1942949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14224079, essv14224078
SamplesHG01817, HG01807
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627142
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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