A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635214



Internal ID7022013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:85889713..85953231hg38UCSC Ensembl
Innerchr14:85889713..85953231hg38UCSC Ensembl
Outerchr14:85889213..85953731hg38UCSC Ensembl
chr14:86356057..86419575hg19UCSC Ensembl
Innerchr14:86356057..86419575hg19UCSC Ensembl
Outerchr14:86355557..86420075hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3863519
hg1963519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15089915, essv15089914
SamplesNA20773, HG02371
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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