A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627329



Internal ID7014159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94823401..94852507hg38UCSC Ensembl
chr11:94556567..94585672hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3829107
hg1929106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv222e214
Supporting Variantsessv14241868
SamplesHG03025
Known GenesAMOTL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627329
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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