A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13769478



Internal ID3771294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45105940..45151354hg38UCSC Ensembl
chr10:45601388..45646802hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3845415
hg1945415
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623083
Supporting Variants
SamplesNA18605
Known GenesRSU1P2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13769478
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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