A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13728166



Internal ID2164775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25898912..25903077hg38UCSC Ensembl
chr10:26187841..26192006hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg384166
hg194166
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622680
Supporting Variants
SamplesHG01956
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13728166
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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