A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592856



Internal ID16380265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:191781711..192023992hg38UCSC Ensembl
Innerchr3:191499500..191741781hg19UCSC Ensembl
Innerchr3:192982194..193224475hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38242282
hg19242282
hg18242282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153416
SamplesHGDP00526
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592856
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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