A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591894



Internal ID16379303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:141851452..141854006hg38UCSC Ensembl
Innerchr3:141570294..141572848hg19UCSC Ensembl
Innerchr3:143052984..143055538hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg382555
hg192555
hg182555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv975061
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591894
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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