A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622996



Internal ID7009853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42116111..42188605hg38UCSC Ensembl
chr10:42611559..42684053hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3872495
hg1972495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13758166, essv13758168, essv13758167, essv13758164, essv13758165, essv13758163
SamplesHG00626, NA18565, HG00428, HG00690, NA18555, HG03653
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622996
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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