A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657771



Internal ID9923876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58100184..58102833hg38UCSC Ensembl
chr14:58566902..58569551hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6289693, essv5783098
SamplesNA18613, NA19004
Known GenesC14orf37
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657771
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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