A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3379630



Internal ID15226602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63132960..63145558hg38UCSC Ensembl
Innerchr9:63133960..63144558hg38UCSC Ensembl
Outerchr9:63131960..63146558hg38UCSC Ensembl
chr9:67037932..67050530hg19UCSC Ensembl
Innerchr9:67038932..67049530hg19UCSC Ensembl
Outerchr9:67036932..67051530hg19UCSC Ensembl
chr9:66777752..66790350hg18UCSC Ensembl
Innerchr9:66778752..66789350hg18UCSC Ensembl
Outerchr9:66776752..66791350hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3812599
hg1912599
hg1812599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4394e59
Supporting Variantsessv8697097
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3379630
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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