A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635042



Internal ID7021842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79188480..79199391hg38UCSC Ensembl
Innerchr14:79188488..79199383hg38UCSC Ensembl
Outerchr14:79188472..79199399hg38UCSC Ensembl
chr14:79654823..79665734hg19UCSC Ensembl
Innerchr14:79654831..79665726hg19UCSC Ensembl
Outerchr14:79654815..79665742hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3810912
hg1910912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15074339
SamplesNA18947
Known GenesNRXN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635042
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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