A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622477



Internal ID6662647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16808207..16934688hg38UCSC Ensembl
chr10:16850206..16976687hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38126482
hg19126482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13706543
SamplesHG00530
Known GenesCUBN, RSU1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622477
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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