A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637227



Internal ID7024021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90409864..90417474hg38UCSC Ensembl
Innerchr15:90409864..90417474hg38UCSC Ensembl
Outerchr15:90409364..90417974hg38UCSC Ensembl
chr15:90953096..90960706hg19UCSC Ensembl
Innerchr15:90953096..90960706hg19UCSC Ensembl
Outerchr15:90952596..90961206hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg387611
hg197611
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317316
SamplesHG02081
Known GenesIQGAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637227
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