A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591563



Internal ID16378972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126986526..127039106hg38UCSC Ensembl
Innerchr3:126705369..126757949hg19UCSC Ensembl
Innerchr3:128188059..128240639hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3852581
hg1952581
hg1852581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv972920
Samples
Known GenesPLXNA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591563
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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