A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592759



Internal ID16380168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188391214..188474598hg38UCSC Ensembl
Innerchr3:188109002..188192386hg19UCSC Ensembl
Innerchr3:189591696..189675080hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3883385
hg1983385
hg1883385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152571
Samples1798860251_A
Known GenesLPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592759
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer