A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3184992



Internal ID11204658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74972132..74972192hg38UCSC Ensembl
chr14:75438835..75438895hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7454559
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3184992
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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