A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3431710



Internal ID15278666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92477165..92477165hg38UCSC Ensembl
Innerchr10:92477164..92477166hg38UCSC Ensembl
Outerchr10:92477115..92477215hg38UCSC Ensembl
chr10:94236922..94236922hg19UCSC Ensembl
Innerchr10:94236921..94236923hg19UCSC Ensembl
Outerchr10:94236872..94236972hg19UCSC Ensembl
chr10:94226902..94226902hg18UCSC Ensembl
Innerchr10:94226903..94226901hg18UCSC Ensembl
Outerchr10:94226852..94226952hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg381388
hg191388
hg181388
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8740704
SamplesNA19240
Known GenesIDE
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3431710
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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