A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697221



Internal ID15061242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64464514..64465712hg38UCSC Ensembl
Innerchr9:64464712..64465514hg38UCSC Ensembl
Outerchr9:64463514..64466712hg38UCSC Ensembl
chr9:69476932..69478130hg19UCSC Ensembl
Innerchr9:69477130..69477932hg19UCSC Ensembl
Outerchr9:69475932..69479130hg19UCSC Ensembl
chr9:68766752..68767950hg18UCSC Ensembl
Innerchr9:68767752..68766950hg18UCSC Ensembl
Outerchr9:68765752..68768950hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3389575
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697221
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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