A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591859



Internal ID16032582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139943096..139985332hg38UCSC Ensembl
Innerchr3:139661938..139704174hg19UCSC Ensembl
Innerchr3:141144628..141186864hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3842237
hg1942237
hg1842237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974776
Samples
Known GenesCLSTN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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