A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8944568



Internal ID13033223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34824561..34824593hg38UCSC Ensembl
Innerchr9:34824570..34824582hg38UCSC Ensembl
Outerchr9:34824538..34824616hg38UCSC Ensembl
chr9:34824558..34824590hg19UCSC Ensembl
Innerchr9:34824567..34824579hg19UCSC Ensembl
Outerchr9:34824535..34824613hg19UCSC Ensembl
chr9:34814558..34814590hg18UCSC Ensembl
Innerchr9:34814579..34814567hg18UCSC Ensembl
Outerchr9:34814535..34814613hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3899
hg1999
hg1899
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3397390
Supporting Variants
SamplesNA07037
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8944568
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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