A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636194



Internal ID7022990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38532935..38533512hg38UCSC Ensembl
Innerchr15:38532943..38533504hg38UCSC Ensembl
Outerchr15:38532927..38533520hg38UCSC Ensembl
chr15:38825136..38825713hg19UCSC Ensembl
Innerchr15:38825144..38825705hg19UCSC Ensembl
Outerchr15:38825128..38825721hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15221219, essv15221220
SamplesNA19023, NA19403
Known GenesRASGRP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636194
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