A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622709



Internal ID6662878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27165209..27189102hg38UCSC Ensembl
chr10:27454138..27478031hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3823894
hg1923894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13732566, essv13732567
SamplesHG04164, HG00631
Known GenesMASTL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622709
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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