A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592449



Internal ID16033172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164959561..165065377hg38UCSC Ensembl
Innerchr3:164677349..164783165hg19UCSC Ensembl
Innerchr3:166160043..166265859hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38105817
hg19105817
hg18105817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8717n54
Supporting Variantsnssv981123
Samples
Known GenesSI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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