A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589854



Internal ID16030577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18430796..18836070hg38UCSC Ensembl
Innerchr3:18472288..18877562hg19UCSC Ensembl
Innerchr3:18447292..18852566hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38405275
hg19405275
hg18405275
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959875
Samples
Known GenesSATB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589854
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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