A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14178525



Internal ID5390318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62000457..62033514hg38UCSC Ensembl
chr11:61767929..61800986hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3833058
hg1933058
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626589
Supporting Variants
SamplesNA18940
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14178525
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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