A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14058287



Internal ID2747316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24209045..24289515hg38UCSC Ensembl
chr11:24230591..24311061hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3880471
hg1980471
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625662
Supporting Variants
SamplesHG02410
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14058287
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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