A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3302444



Internal ID14802705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87127942..87146703hg38UCSC Ensembl
Innerchr15:87128042..87146603hg38UCSC Ensembl
Outerchr15:87127842..87146803hg38UCSC Ensembl
chr15:87671173..87689934hg19UCSC Ensembl
Innerchr15:87671273..87689834hg19UCSC Ensembl
Outerchr15:87671073..87690034hg19UCSC Ensembl
chr15:85472177..85490938hg18UCSC Ensembl
Innerchr15:85472277..85490838hg18UCSC Ensembl
Outerchr15:85472077..85491038hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3818762
hg1918762
hg1818762
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7731572, essv7730953
SamplesNA19238, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3302444
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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