A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14951697



Internal ID6490079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29259610..29267528hg38UCSC Ensembl
Innerchr14:29259610..29267528hg38UCSC Ensembl
Outerchr14:29259110..29268028hg38UCSC Ensembl
chr14:29728816..29736734hg19UCSC Ensembl
Innerchr14:29728816..29736734hg19UCSC Ensembl
Outerchr14:29728316..29737234hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg387919
hg197919
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633927
Supporting Variants
SamplesNA20529
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14951697
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