A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590557



Internal ID16377966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66500277..66501398hg38UCSC Ensembl
Innerchr3:66550701..66551822hg19UCSC Ensembl
Innerchr3:66633391..66634512hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381122
hg191122
hg181122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8363n54
Supporting Variantsnssv964222
Samples
Known GenesLRIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590557
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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