A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634237



Internal ID7021041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42494131..42617243hg38UCSC Ensembl
chr14:42963334..43086446hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38123113
hg19123113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14989579, essv14989580
SamplesHG01162, HG01241
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634237
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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