A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697316



Internal ID13733495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65763615..65779313hg38UCSC Ensembl
Innerchr9:65764615..65778313hg38UCSC Ensembl
Outerchr9:65762615..65780313hg38UCSC Ensembl
chr9:70386732..70402430hg19UCSC Ensembl
Innerchr9:70387732..70401430hg19UCSC Ensembl
Outerchr9:70385732..70403430hg19UCSC Ensembl
chr9:69626552..69642250hg18UCSC Ensembl
Innerchr9:69627552..69641250hg18UCSC Ensembl
Outerchr9:69625552..69643250hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3815699
hg1915699
hg1815699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3388281
Supporting Variants
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697316
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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