A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697419



Internal ID15062211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90162050..90163048hg38UCSC Ensembl
Innerchr9:90162049..90163049hg38UCSC Ensembl
Outerchr9:90161050..90164048hg38UCSC Ensembl
chr9:92924332..92925330hg19UCSC Ensembl
Innerchr9:92924331..92925331hg19UCSC Ensembl
Outerchr9:92923332..92926330hg19UCSC Ensembl
chr9:91964152..91965150hg18UCSC Ensembl
Innerchr9:91965151..91964151hg18UCSC Ensembl
Outerchr9:91963152..91966150hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3377946
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697419
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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