A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3324868



Internal ID15171848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94558259..94558278hg38UCSC Ensembl
Innerchr14:94558255..94558282hg38UCSC Ensembl
Outerchr14:94558236..94558301hg38UCSC Ensembl
chr14:95024596..95024615hg19UCSC Ensembl
Innerchr14:95024592..95024619hg19UCSC Ensembl
Outerchr14:95024573..95024638hg19UCSC Ensembl
chr14:94094349..94094368hg18UCSC Ensembl
Innerchr14:94094372..94094345hg18UCSC Ensembl
Outerchr14:94094326..94094391hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9667458, essv9667424, essv9667435, essv9667447
SamplesNA11931, NA12287, NA12815, NA12874
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3324868
Frequency
Sample Size185
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer