A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3331723



Internal ID15178712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76996772..76996800hg38UCSC Ensembl
Innerchr9:76996784..76996786hg38UCSC Ensembl
Outerchr9:76996758..76996812hg38UCSC Ensembl
chr9:79611688..79611716hg19UCSC Ensembl
Innerchr9:79611700..79611702hg19UCSC Ensembl
Outerchr9:79611674..79611728hg19UCSC Ensembl
chr9:78801508..78801536hg18UCSC Ensembl
Innerchr9:78801520..78801522hg18UCSC Ensembl
Outerchr9:78801494..78801548hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38251
hg19251
hg18251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8945171
SamplesNA18523
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3331723
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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