A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6575079



Internal ID9552482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89461363..89472612hg38UCSC Ensembl
Outerchr14:89461206..89472765hg38UCSC Ensembl
Innerchr14:89927707..89938956hg19UCSC Ensembl
Outerchr14:89927550..89939109hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3811560
hg1911560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666528
Supporting Variants
SamplesHG00236
Known GenesFOXN3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6575079
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