A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13968227



Internal ID4583474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126967806..126984836hg38UCSC Ensembl
chr10:128766065..128783100hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3817031
hg1917036
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624869
Supporting Variants
SamplesHG04096
Known GenesDOCK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13968227
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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