A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665688



Internal ID9931793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:71177189..71178400hg38UCSC Ensembl
Outerchr14:71177152..71178450hg38UCSC Ensembl
Innerchr14:71643906..71645117hg19UCSC Ensembl
Outerchr14:71643869..71645167hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381299
hg191299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6594070
SamplesNA19779
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665688
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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