A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592533



Internal ID16379942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173528784..173583247hg38UCSC Ensembl
Innerchr3:173246574..173301037hg19UCSC Ensembl
Innerchr3:174729268..174783731hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3854464
hg1954464
hg1854464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8733n54
Supporting Variantsnssv981301, nssv981299, nssv981300, nssv981298
Samples
Known GenesNLGN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592533
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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