A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591855



Internal ID16032578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:139001362..139023305hg38UCSC Ensembl
Innerchr3:138720204..138742147hg19UCSC Ensembl
Innerchr3:140202894..140224837hg18UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3821944
hg1921944
hg1821944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv974771
Samples
Known GenesPRR23A, PRR23B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591855
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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