A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592528



Internal ID16379937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173521663..173592563hg38UCSC Ensembl
Innerchr3:173239453..173310353hg19UCSC Ensembl
Innerchr3:174722147..174793047hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3870901
hg1970901
hg1870901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8733n54
Supporting Variantsnssv981283, nssv981282
Samples
Known GenesNLGN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592528
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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