A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623002



Internal ID7009859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42293750..42452381hg38UCSC Ensembl
chr10:42789198..42947829hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38158632
hg19158632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13761339, essv13761340, essv13761338, essv13761342, essv13761341, essv13761343
SamplesHG00626, NA18565, HG00690, NA18555, HG03708, NA20804
Known GenesCCNYL2, LOC441666
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623002
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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