A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7864926



Internal ID13317588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38470241..38470249hg38UCSC Ensembl
Innerchr9:38470243..38470247hg38UCSC Ensembl
Outerchr9:38470239..38470251hg38UCSC Ensembl
chr9:38470238..38470246hg19UCSC Ensembl
Innerchr9:38470240..38470244hg19UCSC Ensembl
Outerchr9:38470236..38470248hg19UCSC Ensembl
chr9:38460238..38460246hg18UCSC Ensembl
Innerchr9:38460240..38460244hg18UCSC Ensembl
Outerchr9:38460236..38460248hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3427544
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7864926
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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