A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7836809



Internal ID14691224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32463889..32463890hg38UCSC Ensembl
Innerchr9:32463864..32463915hg38UCSC Ensembl
Outerchr9:32463863..32463916hg38UCSC Ensembl
chr9:32463887..32463888hg19UCSC Ensembl
Innerchr9:32463862..32463913hg19UCSC Ensembl
Outerchr9:32463861..32463914hg19UCSC Ensembl
chr9:32453887..32453888hg18UCSC Ensembl
Innerchr9:32453913..32453862hg18UCSC Ensembl
Outerchr9:32453861..32453914hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38179
hg19179
hg18179
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308999
Supporting Variants
SamplesNA19239
Known GenesDDX58
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7836809
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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