A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7749052



Internal ID14738062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13605521..13605522hg38UCSC Ensembl
Innerchr9:13605492..13605551hg38UCSC Ensembl
Outerchr9:13605491..13605552hg38UCSC Ensembl
chr9:13605520..13605521hg19UCSC Ensembl
Innerchr9:13605491..13605550hg19UCSC Ensembl
Outerchr9:13605490..13605551hg19UCSC Ensembl
chr9:13595520..13595521hg18UCSC Ensembl
Innerchr9:13595550..13595491hg18UCSC Ensembl
Outerchr9:13595490..13595551hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38305
hg19305
hg18305
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3305494
Supporting Variants
SamplesNA18973
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7749052
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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