A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624992



Internal ID7011839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132451891..132486517hg38UCSC Ensembl
chr10:134265395..134300021hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3834627
hg1934627
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13982891, essv13982890, essv13982889
SamplesHG00096, NA19455, NA19468
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624992
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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