A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550423



Internal ID16337832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38463022..38861502hg38UCSC Ensembl
Innerchr10:38751950..39154633hg19UCSC Ensembl
Innerchr10:38791956..39194639hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38398481
hg19402684
hg18402684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv746859
Samples
Known GenesACTR3BP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550423
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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