A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657436



Internal ID9576855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:80867919..80873804hg38UCSC Ensembl
Outerchr14:80867882..80873854hg38UCSC Ensembl
Innerchr14:81334263..81340148hg19UCSC Ensembl
Outerchr14:81334226..81340198hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg385973
hg195973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6211405
SamplesNA18599
Known GenesCEP128
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657436
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