A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3429584



Internal ID15276540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63596316..63596358hg38UCSC Ensembl
Innerchr10:63596326..63596346hg38UCSC Ensembl
Outerchr10:63596284..63596390hg38UCSC Ensembl
chr10:65356076..65356118hg19UCSC Ensembl
Innerchr10:65356086..65356106hg19UCSC Ensembl
Outerchr10:65356044..65356150hg19UCSC Ensembl
chr10:65026082..65026124hg18UCSC Ensembl
Innerchr10:65026112..65026092hg18UCSC Ensembl
Outerchr10:65026050..65026156hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38285
hg19285
hg18285
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8671861
SamplesNA12892
Known GenesREEP3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3429584
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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