A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697055



Internal ID13661916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62886908..62894506hg38UCSC Ensembl
Innerchr9:62887908..62893506hg38UCSC Ensembl
Outerchr9:62885908..62895506hg38UCSC Ensembl
chr9:66542732..66550330hg19UCSC Ensembl
Innerchr9:66543732..66549330hg19UCSC Ensembl
Outerchr9:66541732..66551330hg19UCSC Ensembl
chr9:66282552..66290150hg18UCSC Ensembl
Innerchr9:66283552..66289150hg18UCSC Ensembl
Outerchr9:66281552..66291150hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg387599
hg197599
hg187599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3336381
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697055
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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