A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3377897



Internal ID15224870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65260727..65260746hg38UCSC Ensembl
Innerchr14:65260725..65260748hg38UCSC Ensembl
Outerchr14:65260706..65260767hg38UCSC Ensembl
chr14:65727445..65727464hg19UCSC Ensembl
Innerchr14:65727443..65727466hg19UCSC Ensembl
Outerchr14:65727424..65727485hg19UCSC Ensembl
chr14:64797198..64797217hg18UCSC Ensembl
Innerchr14:64797219..64797196hg18UCSC Ensembl
Outerchr14:64797177..64797238hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg38225
hg19225
hg18225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8966747, essv8966750, essv8966745, essv8966744, essv8966749, essv8966746
SamplesNA18502, NA18489, NA19257, NA19108, NA19093, NA19102
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3377897
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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