A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3428572



Internal ID14928842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19175802..19175816hg38UCSC Ensembl
Innerchr11:19175809..19175809hg38UCSC Ensembl
Outerchr11:19175795..19175823hg38UCSC Ensembl
chr11:19197349..19197363hg19UCSC Ensembl
Innerchr11:19197356..19197356hg19UCSC Ensembl
Outerchr11:19197342..19197370hg19UCSC Ensembl
chr11:19153925..19153939hg18UCSC Ensembl
Innerchr11:19153932..19153932hg18UCSC Ensembl
Outerchr11:19153918..19153946hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865449
SamplesNA12005
Known GenesZDHHC13
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3428572
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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