A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3428956



Internal ID15275912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63304260..63313758hg38UCSC Ensembl
Innerchr9:63305260..63312758hg38UCSC Ensembl
Outerchr9:63303260..63314758hg38UCSC Ensembl
chr9:67259232..67268730hg19UCSC Ensembl
Innerchr9:67260232..67267730hg19UCSC Ensembl
Outerchr9:67258232..67269730hg19UCSC Ensembl
chr9:66949052..66958550hg18UCSC Ensembl
Innerchr9:66950052..66957550hg18UCSC Ensembl
Outerchr9:66948052..66959550hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg389499
hg199499
hg189499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4398e59
Supporting Variantsessv8697118
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3428956
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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