A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635567



Internal ID7022366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102731326..102737802hg38UCSC Ensembl
Innerchr14:102731326..102737802hg38UCSC Ensembl
Outerchr14:102731201..102737939hg38UCSC Ensembl
chr14:103197663..103204139hg19UCSC Ensembl
Innerchr14:103197663..103204139hg19UCSC Ensembl
Outerchr14:103197538..103204276hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg386477
hg196477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15109985, essv15109987, essv15109986
SamplesHG01048, HG01149, HG01474
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635567
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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