A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3432719



Internal ID15279675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23441567..23441577hg38UCSC Ensembl
Innerchr10:23441570..23441574hg38UCSC Ensembl
Outerchr10:23441560..23441584hg38UCSC Ensembl
chr10:23730496..23730506hg19UCSC Ensembl
Innerchr10:23730499..23730503hg19UCSC Ensembl
Outerchr10:23730489..23730513hg19UCSC Ensembl
chr10:23770502..23770512hg18UCSC Ensembl
Innerchr10:23770509..23770505hg18UCSC Ensembl
Outerchr10:23770495..23770519hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865002
SamplesNA12005
Known GenesOTUD1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3432719
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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