A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591936



Internal ID16379345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145830931..145890504hg38UCSC Ensembl
Innerchr3:145548718..145608291hg19UCSC Ensembl
Innerchr3:147031408..147090981hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3859574
hg1959574
hg1859574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975232, nssv975233
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591936
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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