A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592654



Internal ID16033377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182938822..183025479hg38UCSC Ensembl
Innerchr3:182656610..182743267hg19UCSC Ensembl
Innerchr3:184139304..184225961hg18UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3886658
hg1986658
hg1886658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152556
Samples1780854339_A
Known GenesDCUN1D1, MCCC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592654
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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