A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628121



Internal ID6668265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132280887..132292976hg38UCSC Ensembl
chr11:132150781..132162870hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3812090
hg1912090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317586
SamplesNA20795
Known GenesNTM, NTM-IT
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628121
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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