A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635100



Internal ID7021900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81987399..82027541hg38UCSC Ensembl
Innerchr14:81987425..82027516hg38UCSC Ensembl
Outerchr14:81987374..82027567hg38UCSC Ensembl
chr14:82453743..82493885hg19UCSC Ensembl
Innerchr14:82453769..82493860hg19UCSC Ensembl
Outerchr14:82453718..82493911hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3840143
hg1940143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15080485
SamplesHG02733
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635100
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