A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590282



Internal ID16031005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52054188..52063044hg38UCSC Ensembl
Innerchr3:52088204..52097060hg19UCSC Ensembl
Innerchr3:52063244..52072100hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg388857
hg198857
hg188857
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963062
Samples
Known GenesDUSP7, LINC00696
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590282
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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