A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592372



Internal ID16033095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163001313..163003875hg38UCSC Ensembl
Innerchr3:162719101..162721663hg19UCSC Ensembl
Innerchr3:164201795..164204357hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg382563
hg192563
hg182563
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8701n54
Supporting Variantsnssv979822, nssv979818, nssv979820, nssv979821, nssv979819
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592372
Frequency
Sample Size17421
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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