A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3376829



Internal ID15223802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27823521..27823545hg38UCSC Ensembl
Innerchr9:27823527..27823537hg38UCSC Ensembl
Outerchr9:27823503..27823561hg38UCSC Ensembl
chr9:27823519..27823543hg19UCSC Ensembl
Innerchr9:27823525..27823535hg19UCSC Ensembl
Outerchr9:27823501..27823559hg19UCSC Ensembl
chr9:27813519..27813543hg18UCSC Ensembl
Innerchr9:27813535..27813525hg18UCSC Ensembl
Outerchr9:27813501..27813559hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38192
hg19192
hg18192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8944189, essv8944188, essv8944193, essv8944190, essv8944192
SamplesNA18502, NA18861, NA18582, NA18909, NA18501
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3376829
Frequency
Sample Size185
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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