A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697091



Internal ID13732696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63109360..63132358hg38UCSC Ensembl
Innerchr9:63110360..63131358hg38UCSC Ensembl
Outerchr9:63108360..63133358hg38UCSC Ensembl
chr9:67014332..67037330hg19UCSC Ensembl
Innerchr9:67015332..67036330hg19UCSC Ensembl
Outerchr9:67013332..67038330hg19UCSC Ensembl
chr9:66754152..66777150hg18UCSC Ensembl
Innerchr9:66755152..66776150hg18UCSC Ensembl
Outerchr9:66753152..66778150hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3822999
hg1922999
hg1822999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3451680
Supporting Variants
SamplesNA12892
Known GenesLOC286297
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697091
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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