A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3414582



Internal ID15261541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63797498..63844396hg38UCSC Ensembl
Innerchr9:63798498..63843396hg38UCSC Ensembl
Outerchr9:63796498..63845396hg38UCSC Ensembl
chr9:68393232..68440130hg19UCSC Ensembl
Innerchr9:68394232..68439130hg19UCSC Ensembl
Outerchr9:68392232..68441130hg19UCSC Ensembl
chr9:67883052..67929950hg18UCSC Ensembl
Innerchr9:67884052..67928950hg18UCSC Ensembl
Outerchr9:67882052..67930950hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3846899
hg1946899
hg1846899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697160
SamplesNA12878
Known GenesLOC642236
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3414582
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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