A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591675



Internal ID16379084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129606197..129617902hg38UCSC Ensembl
Innerchr3:129325040..129336745hg19UCSC Ensembl
Innerchr3:130807730..130819435hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3811706
hg1911706
hg1811706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973181
Samples
Known GenesPLXND1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591675
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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