A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688090



Internal ID13371227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46430309..46442914hg38UCSC Ensembl
Innerchr10:46431309..46441914hg38UCSC Ensembl
Outerchr10:46429311..46443914hg38UCSC Ensembl
chr10:47106846..47119444hg19UCSC Ensembl
Innerchr10:47107846..47118444hg19UCSC Ensembl
Outerchr10:47105846..47120444hg19UCSC Ensembl
chr10:46526852..46539450hg18UCSC Ensembl
Innerchr10:46527852..46538450hg18UCSC Ensembl
Outerchr10:46525852..46540450hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3812606
hg1912599
hg1812599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3364982
Supporting Variants
SamplesNA12892
Known GenesLINC00842
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688090
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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