A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3353689



Internal ID15200670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9233744..9233780hg38UCSC Ensembl
Innerchr10:9233755..9233767hg38UCSC Ensembl
Outerchr10:9233721..9233803hg38UCSC Ensembl
chr10:9275707..9275743hg19UCSC Ensembl
Innerchr10:9275718..9275730hg19UCSC Ensembl
Outerchr10:9275684..9275766hg19UCSC Ensembl
chr10:9315713..9315749hg18UCSC Ensembl
Innerchr10:9315736..9315724hg18UCSC Ensembl
Outerchr10:9315690..9315772hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38255
hg19255
hg18255
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8946719
SamplesNA19108
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3353689
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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