A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592041



Internal ID16379450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:150762859..150763346hg38UCSC Ensembl
Innerchr3:150480646..150481133hg19UCSC Ensembl
Innerchr3:151963336..151963823hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38488
hg19488
hg18488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv976754
Samples
Known GenesSIAH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592041
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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