A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14035959



Internal ID3264226
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625449
Supporting Variants
SamplesHG02882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14035959
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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