A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622911



Internal ID7009769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36013793..36040639hg38UCSC Ensembl
chr10:36302721..36329567hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3826847
hg1926847
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13754280
SamplesHG03538
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622911
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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