A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15088143



Internal ID4537265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84784725..84820400hg38UCSC Ensembl
chr14:85251069..85286744hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3835676
hg1935676
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635170
Supporting Variants
SamplesHG04033
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15088143
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