A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591858



Internal ID16032581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139934934..139935397hg38UCSC Ensembl
Innerchr3:139653776..139654239hg19UCSC Ensembl
Innerchr3:141136466..141136929hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38464
hg19464
hg18464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974775, nssv974773, nssv974774
Samples
Known GenesCLSTN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591858
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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