A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7864945



Internal ID13317618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87405642..87405653hg38UCSC Ensembl
Innerchr9:87405647..87405648hg38UCSC Ensembl
Outerchr9:87405637..87405658hg38UCSC Ensembl
chr9:90020557..90020568hg19UCSC Ensembl
Innerchr9:90020562..90020563hg19UCSC Ensembl
Outerchr9:90020552..90020573hg19UCSC Ensembl
chr9:89210377..89210388hg18UCSC Ensembl
Innerchr9:89210382..89210383hg18UCSC Ensembl
Outerchr9:89210372..89210393hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3351389
Supporting Variants
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7864945
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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