A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892724



Internal ID19183544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92198781..92215204hg38UCSC Ensembl
Outerchr15:92192685..92222340hg38UCSC Ensembl
Innerchr15:92742011..92758434hg19UCSC Ensembl
Outerchr15:92735915..92765570hg19UCSC Ensembl
Innerchr15:90543015..90559438hg18UCSC Ensembl
Outerchr15:90536919..90566574hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3829656
hg1929656
hg1829656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789532, essv25790827, essv25790299
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892724
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer