A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592907



Internal ID16380316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192771343..192873527hg38UCSC Ensembl
Innerchr3:192489132..192591316hg19UCSC Ensembl
Innerchr3:193971826..194074010hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38102185
hg19102185
hg18102185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv984349
Samples
Known GenesMB21D2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592907
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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