A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8945200



Internal ID14905752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:78089944..78089975hg38UCSC Ensembl
Innerchr9:78089952..78089967hg38UCSC Ensembl
Outerchr9:78089921..78089998hg38UCSC Ensembl
chr9:80704860..80704891hg19UCSC Ensembl
Innerchr9:80704868..80704883hg19UCSC Ensembl
Outerchr9:80704837..80704914hg19UCSC Ensembl
chr9:79894680..79894711hg18UCSC Ensembl
Innerchr9:79894703..79894688hg18UCSC Ensembl
Outerchr9:79894657..79894734hg18UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38241
hg19241
hg18241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3425610
Supporting Variants
SamplesNA19138
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8945200
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer