A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592906



Internal ID16033629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192728274..192914703hg38UCSC Ensembl
Innerchr3:192446063..192632492hg19UCSC Ensembl
Innerchr3:193928757..194115186hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38186430
hg19186430
hg18186430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8809n54
Supporting Variantsnssv984348
Samples
Known GenesMB21D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592906
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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