A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637228



Internal ID7024022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90501718..90502347hg38UCSC Ensembl
Innerchr15:90501718..90502347hg38UCSC Ensembl
Outerchr15:90501527..90502504hg38UCSC Ensembl
chr15:91044950..91045579hg19UCSC Ensembl
Innerchr15:91044950..91045579hg19UCSC Ensembl
Outerchr15:91044759..91045736hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15317317
SamplesNA19920
Known GenesIQGAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637228
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