A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590552



Internal ID16377961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66500159..66501284hg38UCSC Ensembl
Innerchr3:66550583..66551708hg19UCSC Ensembl
Innerchr3:66633273..66634398hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381126
hg191126
hg181126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8362n54
Supporting Variantsnssv964213
Samples
Known GenesLRIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590552
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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