A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625449



Internal ID7012283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16513065..16527271hg38UCSC Ensembl
chr11:16534612..16548818hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3814207
hg1914207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14035959
SamplesHG02882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625449
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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