A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663717



Internal ID9929822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95995063..95998908hg38UCSC Ensembl
Outerchr14:95994906..95999061hg38UCSC Ensembl
Innerchr14:96461400..96465245hg19UCSC Ensembl
Outerchr14:96461243..96465398hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384156
hg194156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5848934
SamplesHG00556
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663717
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