A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010488



Internal ID7059830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57025345..57025873hg38UCSC Ensembl
Innerchr16:57059257..57059785hg19UCSC Ensembl
Innerchr16:55616758..55617286hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38529
hg19529
hg18529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586820
SamplesHuRef
Known GenesNLRC5
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010488
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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