A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591893



Internal ID16379302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141308772..141356120hg38UCSC Ensembl
Innerchr3:141027614..141074962hg19UCSC Ensembl
Innerchr3:142510304..142557652hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3847349
hg1947349
hg1847349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152545
Samples1780862007_A
Known GenesZBTB38
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591893
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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