A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3308483



Internal ID15155432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70358656..70358657hg38UCSC Ensembl
Innerchr9:70358552..70358761hg38UCSC Ensembl
Outerchr9:70358551..70358762hg38UCSC Ensembl
chr9:72973572..72973573hg19UCSC Ensembl
Innerchr9:72973468..72973677hg19UCSC Ensembl
Outerchr9:72973467..72973678hg19UCSC Ensembl
chr9:72163392..72163393hg18UCSC Ensembl
Innerchr9:72163497..72163288hg18UCSC Ensembl
Outerchr9:72163287..72163498hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38288
hg19288
hg18288
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7836698
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3308483
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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