A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627875



Internal ID6668019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118656448..118708205hg38UCSC Ensembl
chr11:118527158..118578914hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3851758
hg1951757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv234e214
Supporting Variantsessv14293210
SamplesHG02769
Known GenesPHLDB1, TREH
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627875
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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