A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634389



Internal ID7021192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46513876..46526329hg38UCSC Ensembl
Innerchr14:46514376..46525829hg38UCSC Ensembl
Outerchr14:46512876..46527329hg38UCSC Ensembl
chr14:46983079..46995532hg19UCSC Ensembl
Innerchr14:46983579..46995032hg19UCSC Ensembl
Outerchr14:46982079..46996532hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3812454
hg1912454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv399e214
Supporting Variantsessv15003109
SamplesNA20581
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634389
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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