A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624569



Internal ID7011422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111787599..111811012hg38UCSC Ensembl
chr10:113547357..113570770hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3823414
hg1923414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13935669
SamplesHG02778
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624569
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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