A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3406165



Internal ID15253127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87276717..87276789hg38UCSC Ensembl
Innerchr9:87276725..87276779hg38UCSC Ensembl
Outerchr9:87276655..87276851hg38UCSC Ensembl
chr9:89891632..89891704hg19UCSC Ensembl
Innerchr9:89891640..89891694hg19UCSC Ensembl
Outerchr9:89891570..89891766hg19UCSC Ensembl
chr9:89081452..89081524hg18UCSC Ensembl
Innerchr9:89081514..89081460hg18UCSC Ensembl
Outerchr9:89081390..89081586hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386040
hg196040
hg186040
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8945303, essv8945304, essv8945299, essv8945300, essv8945301
SamplesNA12155, NA07347, NA11994, NA10847, NA12144
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3406165
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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