A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697162



Internal ID13662875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63848698..63902496hg38UCSC Ensembl
Innerchr9:63849698..63901496hg38UCSC Ensembl
Outerchr9:63847698..63903496hg38UCSC Ensembl
chr9:68444432..68498230hg19UCSC Ensembl
Innerchr9:68445432..68497230hg19UCSC Ensembl
Outerchr9:68443432..68499230hg19UCSC Ensembl
chr9:67934252..67988050hg18UCSC Ensembl
Innerchr9:67935252..67987050hg18UCSC Ensembl
Outerchr9:67933252..67989050hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3853799
hg1953799
hg1853799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3446385
Supporting Variants
SamplesNA12878
Known GenesLOC642236
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697162
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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