A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3375636



Internal ID15222611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30989611..30989641hg38UCSC Ensembl
Innerchr9:30989623..30989627hg38UCSC Ensembl
Outerchr9:30989595..30989657hg38UCSC Ensembl
chr9:30989609..30989639hg19UCSC Ensembl
Innerchr9:30989621..30989625hg19UCSC Ensembl
Outerchr9:30989593..30989655hg19UCSC Ensembl
chr9:30979609..30979639hg18UCSC Ensembl
Innerchr9:30979625..30979621hg18UCSC Ensembl
Outerchr9:30979593..30979655hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38289
hg19289
hg18289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8944328, essv8944330, essv8944329
SamplesNA18489, NA19114, NA19102
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3375636
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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