A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590293



Internal ID16377702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:52055873..52063044hg38UCSC Ensembl
Innerchr3:52089889..52097060hg19UCSC Ensembl
Innerchr3:52064929..52072100hg18UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg387172
hg197172
hg187172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8325n54
Supporting Variantsnssv963081
Samples
Known GenesDUSP7, LINC00696
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590293
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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