A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv981296



Internal ID16275252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:173528784..173581876hg38UCSC Ensembl
Innerchr3:173246574..173299666hg19UCSC Ensembl
Innerchr3:174729268..174782360hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3853093
hg1953093
hg1853093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592532
Supporting Variants
Samples
Known GenesNLGN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv981296
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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