A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3377734



Internal ID15224707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101647060..101647083hg38UCSC Ensembl
Innerchr14:101647023..101647120hg38UCSC Ensembl
Outerchr14:101647000..101647143hg38UCSC Ensembl
chr14:102113397..102113420hg19UCSC Ensembl
Innerchr14:102113360..102113457hg19UCSC Ensembl
Outerchr14:102113337..102113480hg19UCSC Ensembl
chr14:101183150..101183173hg18UCSC Ensembl
Innerchr14:101183210..101183113hg18UCSC Ensembl
Outerchr14:101183090..101183233hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865784, essv7865783
SamplesNA11992, NA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3377734
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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