A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634905



Internal ID7021705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73391534..73401253hg38UCSC Ensembl
chr14:73858242..73867961hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg389720
hg199720
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15055850, essv15055851
SamplesHG02610, HG02642
Known GenesNUMB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634905
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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