A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8677366



Internal ID15024643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2351290..2351303hg38UCSC Ensembl
Innerchr9:2351282..2351311hg38UCSC Ensembl
Outerchr9:2351269..2351324hg38UCSC Ensembl
chr9:2351290..2351303hg19UCSC Ensembl
Innerchr9:2351282..2351311hg19UCSC Ensembl
Outerchr9:2351269..2351324hg19UCSC Ensembl
chr9:2341290..2341303hg18UCSC Ensembl
Innerchr9:2341311..2341282hg18UCSC Ensembl
Outerchr9:2341269..2341324hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38283
hg19283
hg18283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3440236
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8677366
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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