A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3434461



Internal ID15281415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117562651..117563849hg38UCSC Ensembl
Innerchr10:117562849..117563651hg38UCSC Ensembl
Outerchr10:117561651..117564849hg38UCSC Ensembl
chr10:119322162..119323360hg19UCSC Ensembl
Innerchr10:119322360..119323162hg19UCSC Ensembl
Outerchr10:119321162..119324360hg19UCSC Ensembl
chr10:119312152..119313350hg18UCSC Ensembl
Innerchr10:119313152..119312350hg18UCSC Ensembl
Outerchr10:119311152..119314350hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8687890
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3434461
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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