A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7732576



Internal ID14851751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15984151..15984152hg38UCSC Ensembl
Outerchr9:15984005..15984299hg38UCSC Ensembl
Innerchr9:15984149..15984150hg19UCSC Ensembl
Outerchr9:15984003..15984297hg19UCSC Ensembl
Innerchr9:15974150..15974149hg18UCSC Ensembl
Outerchr9:15974003..15974297hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38295
hg19295
hg18295
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302730
Supporting Variants
SamplesNA19108
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7732576
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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