A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622241



Internal ID6662411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6104698..6319178hg38UCSC Ensembl
chr10:6146661..6361141hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38214481
hg19214481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13687340
SamplesHG01668
Known GenesLOC399715, MIR3155A, MIR3155B, PFKFB3, RBM17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622241
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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