A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634606



Internal ID6674723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57401494..57401956hg38UCSC Ensembl
Innerchr14:57401494..57401956hg38UCSC Ensembl
Outerchr14:57401269..57402205hg38UCSC Ensembl
chr14:57868212..57868674hg19UCSC Ensembl
Innerchr14:57868212..57868674hg19UCSC Ensembl
Outerchr14:57867987..57868923hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38463
hg19463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15024589
SamplesNA12749
Known GenesNAA30
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634606
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