A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591669



Internal ID16032392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129566332..129606197hg38UCSC Ensembl
Innerchr3:129285175..129325040hg19UCSC Ensembl
Innerchr3:130767865..130807730hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3839866
hg1939866
hg1839866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973175
Samples
Known GenesPLXND1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591669
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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