A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624369



Internal ID6664536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101084806..101212566hg38UCSC Ensembl
chr10:102844563..102972323hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38127761
hg19127761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13913032
SamplesHG01709
Known GenesTLX1, TLX1NB
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624369
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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