A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697211



Internal ID13733130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64413314..64418012hg38UCSC Ensembl
Innerchr9:64414314..64417012hg38UCSC Ensembl
Outerchr9:64412314..64419012hg38UCSC Ensembl
chr9:69425732..69430430hg19UCSC Ensembl
Innerchr9:69426732..69429430hg19UCSC Ensembl
Outerchr9:69424732..69431430hg19UCSC Ensembl
chr9:68715552..68720250hg18UCSC Ensembl
Innerchr9:68716552..68719250hg18UCSC Ensembl
Outerchr9:68714552..68721250hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg384699
hg194699
hg184699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3343851
Supporting Variants
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697211
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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