A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2904901



Internal ID10577881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73531296..73551296hg38UCSC Ensembl
Innerchr14:73998000..74018000hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3820001
hg1920001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7174468
SamplesHuRef
Known GenesACOT1, HEATR4
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2904901
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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