A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589453



Internal ID16030176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4527782..4725578hg38UCSC Ensembl
Innerchr3:4569466..4767262hg19UCSC Ensembl
Innerchr3:4544466..4742262hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38197797
hg19197797
hg18197797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958051
Samples
Known GenesITPR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589453
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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