A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7744134



Internal ID13850971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102516411..102516412hg38UCSC Ensembl
Innerchr9:102516321..102516502hg38UCSC Ensembl
Outerchr9:102516320..102516503hg38UCSC Ensembl
chr9:105278693..105278694hg19UCSC Ensembl
Innerchr9:105278603..105278784hg19UCSC Ensembl
Outerchr9:105278602..105278785hg19UCSC Ensembl
chr9:104318514..104318515hg18UCSC Ensembl
Innerchr9:104318605..104318424hg18UCSC Ensembl
Outerchr9:104318423..104318606hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38172
hg19172
hg18172
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306475
Supporting Variants
SamplesNA18510
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7744134
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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